nAA. MAY7-19W CLASS BOOK OF ECONOMIC ENTOMOLOGY LOCHHEAD M^ i-'. i^BSk w j| ^ Jk^ T. W. Harris Asa Fitch TowNEND Glover B. D. Walsh C. V. Riley W. Saunders J. Fletcher C. J. S. Bethune Some Pioneer Workers in Economic Entomology. Si CLASS BOOK ^l^ OF /J- ECONOMIC ENTOMOLOGY WITH SPECIAL REFERENCE TO THE ECONOMIC INSECTS OF THE NORTHERN UNITED STATES AND CANADA BY WILLIAM LOCHHEAD, B. A., M. S. (Cornell) PROFESSOR OF BIOLOGY IN THE MACDONALD COLLEGE OF McGILL UNIVERSITY; F. A. A. S. MEMBER OF THE ENT. SOC. OF AMERICA, AND THE AM. ASSOC. ECON. ENT.; EX-PRESIDENT ENT. SOC. OF ONTARIO; PRESIDENT QUEBEC SOC. FOR THE PROTECTION OF PLANTS, ETC. WITE 257 ILLUSTRATIONS PHILADELPHIA BLAKISTON'S SON & CO. 1012 WALNUT STREET Copyright, 1919, by P. Blakiston's Son & Co. THE MAPX.H! FRBBS X O R K PA, PREFACE All teachers are agreed that the best results in the classroom are secured only by the adoption of the best pedagogical methods, with ready access to the necessary specimens and literature. Just what these methods comprise, however, is, with many teachers, a matter of opinion. Quot homines tot sententice, nevertheless the indulgent reader may concede that an experience of over twenty years as a teacher of economic entomology in agricultural colleges may warrant the voicing of the author's conviction that instruction in this subject should con- sist of (i) studies on the structure, metamorphosis, and bionomics of insects, carried on both in the laboratory and in the field; (2) practice in the classification and description of the more common insects in their various stages; and (3) studies of the methods of control, with practical exercises in the preparation and application of insecticides. Although several most excellent manuals on Economic Entomology have been published in recent years, there seems to be a need for a book providing the necessary information for the student in the class- room, laboratory and field along the lines indicated above. This class-book, therefore, has been prepared to meet the needs of the class-room instructor, and his needs have influenced the mode of presentation of the subject material. It does not presume to take the place of the invaluable and well-known works of Folsom, Comstock, Slingerland and Crosby, and others; but rather, it aims to present such material as will best help the student in acquiring a fair working knowl- edge of the modern science of Economic Entomology. The treatment of many of the topics is necessarily limited, and the keys for the identification of orders, families, and genera make no pre- tensions to completeness. The descriptions of the species discussed in Part III are stripped of all unnecessary verbiage so that all the essential facts of the life-histories may be included in the space at the author's disposal. VI PREFACE Laboratory exercises have been omitted, as the intelligent teacher is in a better position than the author to prepare practicums adapted to local conditions. It was thought advisable to limit the species discussed mainly to those belonging to the Northern United States and Canada, i.e., to the Canadian, Transition, and Upper Austral Zones. It was also deemed advisable to make but brief mention of the insects affecting forest trees. Students interested in such studies are referred to the recent bulletins of A. D. Hopkins of Washington and J. M. Swaine of Ottawa for the results of the latest investigations. The author is indebted to many fellow-teachers and workers for valu- able aid and suggestions in the preparation of this book. In most respects it is a compilation from recent text-books, bulletins, and arti- cles. In a work of this kind errors are likely to appear in spite of every precaution, but considerable care has been taken to reduce them to a minimum. Special mention must be made of the kindness of many authors and publishers in furnishing illustrations, and the writer here thanks his friend and teacher. Professor J. H. Comstock of Cornell University, for permission to use illustrations of wing- venation from his recent work, "The Wings of Insects;" Dr. C. G. Hewitt, Dominion Entomolo- gist, for free use of cuts from the publications of the Canadian Ento- mological Branch; Dr. L. O. Howard, Chief of the U. S. Bureau of Entomology, for many electrotypes of the Bureau illustrations; Pro- fessor J. H. Sanders of the Pennsylvania Agricultural Experiment Station, for permission to use his admirable figures of pygidia of scale insects; Mr. J. J. Davis, Federal Agent of the U. S. Bureau of Entomol- ogy, Lafayette, Indiana, for several photographs of breeding cages, etc.; Professor L. Caesar of the Ontario Agricultural College, and Dr. S. Hadwen, Dominion Pathologist, Health of Animals Branch, Ottawa, for furnishing several cuts; Mr. Arthur Gibson, Entomological Branch, Ottawa; Professor W. H. Brittain of the Truro Agricultural College; Professor P. J. Parrott of the New York Agricultural Experiment Station; Professors Herrick, Crosby and Johannsen of Cornell Univer- sity; Professor W. A. Riley of the Minnesota Agricultural College; Dr. Edith Patch of the Maine Agricultural Experiment Station; Professor W. E. Britton of the Connecticut Agricultural Experiment Station; Professor V. L. Kellogg of the Leland Stanford Jr. University, Professor PREFACE Vll W. B, Herms of the University of California; and the MacMillan Co., the Comstock PubHshing Co., Henry Holt and Co., and P. Blakiston's Son and Co., for permission to use certain illustrations from their entomological publications. To Mr. E. M. DuPorte, M. Sc, of Macdonald College, the author is specially indebted for the drawings illustrative of the structure of insects in Part I, for valuable criticisms, and for substantial help in proof-reading. W. LOCHHEAD. Macdonald College. CONTENTS INTRODUCTION PART I— THE STRUCTURE, GROWTH AND ECONOMICS OF INSECTS Page The Branch Arthropoda i The Class Insecta 2 Structure of Insects 2 External Anatomy 2 Internal Anatomy 19 The Development of Insects 30 Embryology, Metamorphosis — stages 30 Losses due to Insects 38 Beneficial Insects 39 Insects and Birds 44 Insects and Plants 45 Insects as Plant Disease Carriers 46 Insects and Disease 49 Insect Behavior toward Stimuli 57 Relation of Insects to Temperature and Humidity 59 Distribution of Insects 60 Methods of Studying Economic Insects 64 PART II.— THE IDENTIFICATION OF INSECTS INJURIOUS TO FARM, GARDEN AND ORCHARD CROPS, ETC. Insects injurious to Cereal Crops 71 Insects injurious to Indian Corn or Maize 72 Insects injurious to Clover and Alfalfa ' 73 Insects injurious to Peas and Beans 74 Insects injurious to Stored Grain Products 74 Insects injurious to Root Crops 76 Insects injurious to the Potato Crop 76 Insects injurious to Garden Vegetables 77 Insects injurious to the Apple 77 Insects injurious to the Plum 80 Insects injurious to the Cherry 82 Insects injurious to the Peach 83 Insects injurious to the Raspberry and Blackberry 83 Insects injurious to the Gooseberry and Currant 84 ix X CONTENTS Pace Insects injurious to the Grape 85 Insects injurious to the Strawberry 86 Insects affecting Shade Trees 87 Insects injurious to Greenhouse plants 90 Insects affecting Domestic Animals 90 Insects of the Household 92 PART III.— CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS Common Orders 93 Aptera group 94 Thysanura 95 Neuropteroida group 96 Mallophaga 100 Orihopteroida group 102 Isoptera 102 Corrodentia 103 Blattoidea 103 Mantoidea 105 Dermaptera 106 Phasmoidea 106 Orthoptera 107 Thysanoptera 118 Homoptera 122 Hemiptera 158 Siphunculata 167 Lepidoptera 169 Diptera 239 Siphonaptera 279 Coleoptera 280 Hymenoptera 343 Invertebrates other than Insects 363 PART IV.— THE CONTROL OF INJURIOUS INSECTS Factors of Insect Control 373 Methods of Control 374 The Action of Insecticides 400 Utilization of Parasitic Insects 401 Bibliography 407 Glossary . . . . 409 Index 415 INTRODUCTION 'Economic Entomology is that phase of Entomology which relates to the control of injurious insects. Its scope is much wider than that of applied entomology, for the latter, properly speaking, is the application of the principles that have been formulated by the economic entomolo- gist as a result of his investigation of insects and their relations to their environment. Its scope embraces a study of the structure, habits and life-histories of the injurious insects and of their relations to all the natural and artificial conditions to which they may be subjected. It also includes the investigation of the nature of the losses and the prac- ticable means by which they may be prevented or lessened. Considering the great variety of insect forms, their diverse methods of food habits, the large number of kinds of hosts which supply them with food, and the enemies which tend to destroy them, it becomes evident that the problem of insect control is most complex. As Professor Forbes says: " The subject matter of this science is not insects alone, nor plants alone, nor farming alone. One may be a most ex- cellent entomologist or botanist, or he may have the whole theory and practice of agriculture at his tongue's end, and at his fingers' end as well, and yet be without knowledge or resources when brought face to face with a new practical problem in economic entomology. The subject is essentially the relation of these things to each other; of insect to plant and of plant to insect, and of both of these to the purposes and opera- tions of the farm, and it involves some knowledge of all of them." The Rise of Economic Entomology The records of the rocks reveal the existence of insects at an early period in the world's history, long before man made his appearance. Early historic records also show clearly that not only man himself but also his crops and flocks sufifered from insect attacks. The ravages of locusts, canker worms and palmer worms are frequently described in graphic language by the Old Testament prophets. Xll INTRODUCTION In America, too, before the advent of Europeans, the Indians were acquainted with insects that injured their corn fields, and during the seventeenth and eighteenth centuries the crops of the early settlers were seriously ravaged by "canker worms" and grasshoppers. One may say, therefore, with Webster: "the actual economic element in entomology is inevitably as old as Agriculture itself." On account, however, of the ignorance and superstition that prevailed even among the learned classes regarding the nature and habits of insects, no progress in the control of insect pests was made or was possible until the latter half of the nineteenth century. The introduction of rational methods of control had to wait until considerable advance had been made in the classification of insects and in a knowledge of their structure, habits and life-history. In so far as America is concerned, it may be said that outbreaks of certain insects, viz., the Rocky Mountain locust, the cotton worm and the Colorado potato beetle during the last quarter of the nineteenth century produced wide-spread attention to the great losses caused by them, and forced the U. S. government at that time to appoint a commission of entomological specialists for the purpose of investi- gating the conditions. It was during this period that some of the modern insecticides and improved spraying machinery were introduced, Paris green becoming the standard remedy against the Colorado potato beetle and the cotton worm, and kerosene emulsion against sucking insects. The reports of Harris, Fitch and Riley, especially those on the Rocky Mountain locust laid the foundation for future ecological studies when the relations of injurious insects to other organisms and to external factors were closely investigated. About the beginning of this century the San Jose scale and the cotton boll-weevil threatened two important industries, and as a result of the investigations many advances were made in the use of spraying machinery and insecticides, notably lime-sulphur wash and hydrocyanic acid gas, and in the application of biological processes and principles. In the attempt to solve the problem of the control of the gypsy and brown-tail moths during the last twelve years another very important advance was made toward a better understanding of parasitic insects and of the part they are likely to play in the control of insects in the future. Regarding the outlook of fighting insects along this line Dr. Howard says: "There will be a very considerable development of this INTRODUCTION Xlll method of warfare against injurious insects in the future. It should be termed "the biological method of fighting insects" and, looking at the problem in a broad way, so far as this country is concerned, when we consider that more than one-half of our principal crop pests have been accidentally imported from other countries, there seems no reason why a systematic study of a very large number of parasitic and predatory insects native to the countries from which these pests were accidentally imported should not be made with a view of ultimate importation of all of them into the United States. In fact, since there exist all over the world beneficial insects, many of which can undoubtedly be accli- matized here, and some of which will undoubtedly prove of value to American agriculture, carefully planned work should be begun looking to the ultimate increase of our insect population by the addition of as many of these beneficial forms as possible. Of course this would mean a very great amount of careful biological study in the countries of origin by men specially trained in this sort of work, if results of value are to be obtained. Strikingly beneficial results could not be expected speedily, and, in fact, we might not be able for many years to estimate the bene- fits derived from such a service; but it seems clear that we should have in this country as many of these surely beneficial forms as can be acclimatized." The greatest impetus to the development of economic entomology was perhaps the establishment of Experiment Stations and Agricultural Colleges where courses of instruction were given in this branch of zoology, and where hundreds of students have been trained to undertake investigations of the many insect problems that were awaiting solution. An interesting feature of the latest development in the study of inju- rious insects is the method of investigation that has been adopted in most entomological stations. "Field stations" where the insects are studied under both field and laboratory conditions are established in infested areas, each in charge of an expert and a staff of assistants. These officers also keep in close touch with the insect conditions of the district, and are often able to "test out" control measures at many places by interesting the farmers and orchardists in the valuable work they are conducting. Even in a sketch of the main features of the rise of American eco- nomic entomology, such as this is, mention must be made of some of the pioneer entomologists who laid firmly and well the foundations of XIV INTRODUCTION this modern science. Dr. T. W. Harris (i 759-1856) in Massachusetts, Dr. Asa Fitch (1809-1879) in New York, Townend Glover at Washing- ton, B. D. Walsh (1808-1869), Dr. C. V. Riley (1843-1895) in Missouri and at Washington, Dr. W. Le Baron and Cyrus Thomas in Illinois, and Dr. W. Saunders (1835-1914), Dr. C. J. S. Bethune (1838 ) and Dr. James Fletcher (1852-1908) in Canada stand out prominently on account of the excellent investigations of the life-histories of injurious insects and their careful determination of effective methods of control. {See frontispiece.) ECONOMIC ENTOMOLOGY PART I THE STRUCTURE, GROWTH AND ECONOMICS OF INSECTS BRANCH ARTHROPODA (Arthropods) Crabs, crayfish and lobsters, spiders and scorpions, centipedes and millipeds have in common with insects jointed appendages and seg- mented, bilaterally symmetrical bodies with a chitinized external skeleton (exo-skeleton) — distinguishing characteristics of the great branch Arthropoda of the Invertebrate animals. These near relatives of insects may be grouped into four classes: 1. Crustacea. — Aquatic, gill-breathing, wingless Arthropods with two pairs of antennae and at least five pairs of legs. Examples: Crabs, crayfish, lobsters, shrimps, sow-bugs, etc. 2. Arachnida. — Air-breathing, wingless Arthropods without anten- nae, and usually with four pairs of legs. Examples: Spiders, mites, ticks, and scorpions. 3. Diplopoda. — Air-breathing, wingless Arthropods with one pair of antennae and numerous body segments each of which bears two pairs of legs. The mouth-parts consist of a pair of mandibles and a compound plate. Example: Millipeds. 4. Chilopoda. — Air-breathing, wingless Arthropods with one pair of antennae and numerous body segments each bearing one pair of legs. The mouth-parts consist of one pair of mandibles and two pairs of maxiUas. Example: Centipedes. (Classes 3 and 4 are frequently grouped as sub-classes of the class Myriapoda.) 2 ECONOMIC ENTOMOLOGY Class Insecta (Insects) The Hexapoda or Insecta are air-breathing Arthropoda with one pair of antennae, three pairs of legs, and usually one or two pairs of wings in the adult state. Insects form a well-defined class of animals, remarkable for the large number of species. The abundance of some species is so great that frequently they constitute a menace to the life of plants upon which they feed. The economic importance of insects is being rapidly realized by the public in recent years on account of the prominence given to the part taken by the common house fly in the spread of typhoid fevers and other diseases, the mosquitoes in malaria and yellow fever, the San Jose scale and codling worm in orchards, the boll-weevil in cotton fields, the army worm and hessian fly in grain fields, the tent caterpillar and bark beetles in orchards and forests, and many other pests that are causing much annoyance, danger and loss. The Structure of Insects EXTERNAL ANATOMY The body of the insect is bilaterally symmetrical and is divided into three distinct parts — the head, the thorax and the abdomen, each composed of a number of segments separated by membranous portions (Fig. i). Each segment again is made up of a number of sclerites, hardened plates separated from each other by seams or impressed lines known as sutures. The skeleton is external, and is in form a hollow cylinder with the muscles attached within. The skin layer or cuticle is laminated, consisting of two layers secreted by the underlying hypodermal cells. The hard tough texture of the skin is due to chitin, an organic substance resembling that which gives the characteristic texture to horns and hoofs. (a) Head. — The skeleton of the head or skull is composed of six or seven closely united segments, and carries the eyes and antennce. The mouth is situated on the front ventral surface. The following regions can be easily recognized: STRUCTURE, GROWTH AND ECONOMICS OF INSECTS Epicranium (a) Vertex or crown, the summit of the head, often with ocelh. (b) Front or face. (c) Genae or cheeks. (d) Occiput, which surrounds the posterior opening of the skull. (e) Clypeus, to which the labrum or upper lip is attached, (/) Gula, to which the labium or lower lip is attached (see Figs. 2 and 3). ForeiV/ng ,v Mmdmn< Fig. I. — Diagram showing the position and arrangement of the principal organs and appendages of an insect. Ant., Antenna; Br., brain; Ao., aorta; LM., leg mus- cles originating in the thorax; DM., dorsal longitudinal muscles of abdomen; H., heart; MT., Malpighian tubules; ED., efferent duct (oviduct or vas deferens) of reproductive system; G., gonad (ovary or testis); Cer., cercus; A., anus; Gon., gonapophyses; CD., common duct (vagina or seminal vesicle) of reproductive sys- tem; VG., ganglia of ventral nerve chain; Tr., tracheal trunk showing origin and distribution of ventral, dorsal and visceral tracheal branches; VM., ventral longi- tudinal muscles; TS., tergo-sternal muscles; Cox., coxa; Tro., trochanter; Fetn., femur; Tib., tibia; Tar., tarsus; SGL, salivary gland; SD., salivary duct; SG., sub- cesophageal ganglion; Ph., pharynx; S., stomodfEum or fore intestine; M., mesen- teron or mid intestine; P., proctodaeum or hind intestine. In addition there is in the head an internal chitinous skeleton called the tentorium, which acts as a supporting structure. It varies in form in different insects. but consists essentially of a central plate and two pairs of arms connecting with the skull. (The tentorium may be isolated by boiling the head in a 5 per cent, solution of caustic potash for ten minutes.) Mouth-parts. — In general there are three types of mouth-parts: mandibulate, present in the generalized orders and in the Orthoptera, ECONOMIC ENTOMOLOGY Pig. Fig. 3. a.. Antenna; E Fig. 2. — Cephalic view of the head of cricket, a.. Antenna; e., compound eye; epicranium; 6.1. , lateral ocellus; o.m., median ocellus; e.s., sutures of the epi- cranium; C, gena; Cp., C.a., clypeus; L., labrum; Md., mandible; p.m., maxillary palpus; p.l., labial palpus. Fig. 3. — Caudal view of head of cricket. E., Epicranium; 0., occiput; P.P., occipital foramen; P.G., postgena; SM., submentum; M., mentum; gl., glossa; pgl., paraglossa; pg., palpiger; pi., labial palpus; C.i, C.2., cardo, pf., palpifer; g., galea; s., stipes; I., lacinia; p.m., maxillary palpus; md., mandible. Fig. 4. — Labrum and clypeus of cricket. STRUCTURE, GROWTH AND ECONOMICS OF INSECTS Ephemerida, and Coleoptera; suctorial, present in the Hemiptera, Lepidoptera and Diptera; and mandihulate-suctorial in the Hymen- optera. The mouth-parts with the exception of the labrum are true appendages of the head segments, and in the embryo arise in exactly the same way as the legs and antennas. Mandibulaie Mouth-parts. — The mouth-parts of biting insects consist of: the labrum or upper lip attached to the clypeus (Figs. 2 and 4) ; a pair of mandibles, simple and unjointed, articulated to the gencB; a pair of maxillcB, each made up of a basal one-, or two-jointed p.m. Fig. 5. Fig. 6. Fig. 5. — Mandible of cricket. A, Cephalic view; B, caudal view; mh., mem- brane; mc.i, mc.2, adt., adductor muscles; abt., abductor muscles. Fig. 6. — Maxilla of cricket. C.i, C.2, Cardo; Mb.2, base of maxilla; pf., pal- pifer; st., stipes; p.m., maxillary palpus; g., galea; /., lacinia. hinge segment, the cardo, a central segment the stipes which bears the palpifer to which the typically five-jointed palpus is attached, and two distal lobes the outer of which is termed the galea and the inner the lacinia (Fig. 6). The labium or lower lip, composed of a broad basal part, the submenfum, joined to the gula, a mentum or central portion, a pair of jointed palpi attached to the mentum by means of a small sclerite, the palpiger, and a median part which may be simple or slightly bilobed in which case it is termed the ligula, or it may consist ECONOMIC ENTOMOLOGY of a distinct pair of inner and outer lobes termed respectively the glosscB and paraglosscB (Figs. 3 and 7). A comparison of Figs. 6 and 7 will show a perfect homology between the segments of the maxillae and of the labium. The hypopharynx or tongue united to the base of the labium; and the epipharynx under the labrum and clypeus bearing teeth, tubercles or bristles (Figs. 8 and 9). These parts diflfer greatly in the different orders. Suctorial Mouth-parts. — The suctorial mouth-parts of flies, bugs, moths and other insects have been evolved from the primitive mandibu- late type. In some forms such as the squash bug and mosquito all of the mouth-parts are present and it is comparatively easy to identify them with the corresponding append- ages of the biting insects. In other forms, however, the house-fly for ex- T^^^^PSrf ample, some of the mouth-parts are missing or fused with others, and it is Fig. 7. Fig. 8. Fig. 7. — Labium of cricket, hyp., Hypopharynx; gl., glossa; pi., labial palpus; pg., palpiger; m., mentum; sm., submentum. Pig. 8. — The labrum-epipharynx of cricket. I., paraglossa; more difficult to determine their homology. The following descrip- tions will illustrate the typical arrangements in the three chief purely suctorial orders of insects. Three types occur in the Diptera — the piercing type, with all the mouth-parts present, e.g., the female horse fly and mosquito; the piercing type with some of the mouth-parts missing or fused, e.g., the horn flies and stable flies, and the non- piercing type such as the house-fly and blow flies in which the beak is used for rasping and sucking. Mouth-parts of the Horse Fly (Tabanid). — The mouth-parts of the female are composed of six blades loosely ensheathed in the labium STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 7 which is the conspicuous median portion terminating in a large labellum (Fig. id). The mandibles are flat and sword-Hke; the maxillae are narrower, but with broad conspicuous palpi; the hypo pharynx and labrum-epipharynx are also narrow and lancet-like. ad.md. depJb. Pig. 9. — Front of head of Gryllus pennsylvanictis with face and vertex removed. Upper Figure. — Epic, Epicranium; Ad., prd.. Id., dilator muscles of the pharynx; Md., mandible; Ph., pharynx. Lower Figure. — Longitudinal dorsoventral section through the head of Gryllus pennsylvanictis. prd., prd. 2, prd.3, pstd., Vd., Dilators of the pharynx; Oc, ocellus; Ad.md., adductor of the mandible; Dep.hyp., depressor of the hypopharynx; Hyp., hypopharynx; r.hyp., retractor of the hypopharynx; ap.lb., apodeme of the labium; r.hyp., retractor of the hypopharynx; Jl.st., flexor of the stipes; T.C., central plate of the tentorium. Mouth-parts oj Mosquito. — The mouth-parts are similar in number to those of the horse fly but they are more bristle-like (Fig. 11). Mouth-parts of the House-fly. —When the head of a living house-fly is pinched between the thumb and finger the mouth-parts are protruded to their full length. They constitute a soft "proboscis" enlarged at 8 ECONOMIC ENTOMOLOGY the tip into a pair of soft cushion-like lobes, the oral lobes or lobelia (Fig. 12). The under sides of these lobes are traversed by a large number of open channels, the pseudo-trachece, which open into the mouth situated near the middle; the greater portion of this proboscis is the modified labium. Lying above the grooved labium is the small spade- like labrum which may be raised by a pin. Near the base of the probos- cis and above the labrum are two small lobes, the maxillary palpi, the maxillae being fused with the fleshy base of the labium. Fig. 10. — Head and mouth-parts of a horse-fly (Tabanus). The maximum number of parts is retained, but the piercing structures are distinctly blade-hke. Dipteron type, second subtype. A, Side view of head showing: i, antenna (brachy- cerous); 2, compound eye; 3, labium; 4, labella; 5, maxillary palpus; B, piercing structures exposed, labium removed; 6, mandibles; 7, maxillae; 8, hypopharynx; 9, labrum-epipharynx. {After Herms.) Mouth-parts of the Stable Fly. — The proboscis is awl-shaped and is adapted for both piercing and sucking (Fig. 13). It projects forward horizontally and has a prominent elbow. The labella are small and are provided with cutting and adhesive structures. Lying above and within the folds of the proboscis or labium are two unequal, sharp heavy bristles, the larger representing the labrum and the smaller the hypo- pharynx. The maxillary palpi are not so large as those of the house- fly. The palpi of the Horn Fly are longer and more flattened, and the proboscis is plumper and not thrown so far forward. Mouth-parts of the Squash Bug. — -The mandibles and maxillae are reduced to needle-like structures, the two innermost (the maxillae) are united to form a piercing tube. The needles fit in the groove of the STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 9 jointed beak, the modified labium. The labrum closes the base of the groove (Fig. 14). I li h Fig. II. — Mouth-parts of female mosquito (Culex pipiens). A, Dorsal aspect; B, transverse section; C, extremity of maxilla; D, extremity of labrum-epi- pharynx; a., antenna; e., compound eye; h., hypopharynx; I., labrum-epipharynx; li., labium; m., mandible; mx., maxilla; p-, maxillary palpus. {After Folsom and Dimmock.) Fig. 12. — Mouth-parts of the house-fly (Musca domestica). lb., Labrum; tnx.p., maxillary palpi; li., labium; la., labellum. {After Kellogg.) Mouth-parts of the Butterfly. — The long sucking tube is composed of the two maxillae joined together, while the other mouth-parts are rudimentary (Fig. 15). lO ECONOMIC ENTOMOLOGY Mandibulate-siidorial Mouth-parts. — Among the Hymenoptera we find a combination of the two types — well-developed biting mandibles and a labium or hypopharynx fitted for sucking or lapping liquid food. In ants and sawflies the mandibles are more in evidence, while the bees and wasps have well-developed sucking apparatus. Ants use their mandibles for various purposes, including the comminution of food, building of nests, transportation of larvae, slaves, etc., and in attack and defence against their enemies; the hypopharynx is used in lapping Hquid food. Selat Lahruin Jhealh, = labium Jetae,- Mandible and AloxiUot, Fig. 13. Fig. 14. Fig. 13. — Side view of the head and mouth-parts of the stable fly {Stomoxys calci- trans). Stylets reduced in number and closely ensheathed by the labium, i. Antenna; 2, compound eye; 3, labium; 4, labella; 5, labrum; 6, hypopharynx; 7, maxillary palpi. {After Herms.) Fig. 14. — Beak of a hemipteron. {After Riley and Johannsen.) Mouth-parts of the Honey Bee. — These consist of the labrum and epipharynx above with the short trowel-like mandibles on each side for moulding wax; the maxilla forming conspicuous lateral wings with the galea and lacinia fused into one piece, and the palpi minute (Fig. 16). The labium is the long portion on each side of the tongue and ends in a pair of palpi. The middle tongue is the hypopharynx ending in a small labellum. Antennae. — ^The antennae or feelers are sensory organs, and are very variable in structure. They carry the organs of touch, and probably those of smell and hearing in some cases. On the surface of some of the STRUCTURE, GROWTH AND ECONOMICS OF INSECTS II segments are fine hairs, connected below with nucleated nerve cells, which are believed to be tactile hairs. There are too in some cases pits or oval depressions, also connected with a nerve cell, which are thought to be gustatory organs. Other pits situated in patches at the lower end of the segments are beheved to be auditory organs. Eyes. — The eyes of insects are of three kinds: simple, compound and agglomerate. The simple eyes or ocelli appear externally as a single convex lens, and are borne by the most primitive insects such as the Collembola, all eyed larvae, and in the adults of most of the winged insects. In winged forms there are usually three, supple- mentary to the compound eyes, and borne on the vertex or on the front, arranged generally in a triangle. The agglomerate eye is a compound eye in which the facets are not fused but well separated from each other, e.g., male Coccids. Organs of Hearing.- — Several kinds of auditory organs occur in insects and these are variously located. In locusts they are tympanic membranes, located on the base of the abdomen; in the katydids and crickets on the tibiae of the fore legs. In the mosquitoes and many other groups certain sensitive hairs on the antennae serve to take up and transmit sound waves. Organs of Smell.— These organs are butterfly (Vanessa), a., ° ^ , tennse; /., labial palpi; p., variously located — on the antennae in flesh boscis. (After Foisom.) flies, ants, bees and wasps, some moths and beetles; on the maxillary and labial palpi in Perla and Silpha; and on the cerci in the cockroach and some Orthoptera. Organs of Taste. — Taste organs are also variously located — on the hypopharynx in the honey bee, on the epipharynx of most biting insects, and on the maxillary palpi in wasps. All sense organs consist essentially of the following parts: (i) a nerve of the central nervous system communicating with (2) one or two modified hypodermal cells, and (3) external supporting or accessory structures such as setce, tubercles or pits. Fig. I 5 -Head of a An- pro- 12 ECONOMIC ENTOMOLOGY Fig. i6. — Head and mouth-parts of the honey bee {Apis melliferd). Both types of mouth-parts well developeti but the mandibles are used chiefly for portage and modeling (Hymenopteron type). A, Front view of the head showing: i, antennae; 2, compound eyes; 3, simple eye; 4, labrum; 5, mandibles; 6, maxillae (lacinia); 7, labium (palpi only); 8, hypopharynx(?); B, mouth-parts removed to show the parts; 5, mandibles; 6, maxillae (lacinia); 7, labium (palpi only); 8, hypopharynx (?); 9, bouton; lo, maxillary palpus; 11, mentum; 12, submentum; 13, cardo; 14, stipes. {After Hertns.) Fig. 17. — Section through the thorax of an insect. L., Leg; P., pleuron; S., sternum; T., tergum; W., wing. STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 13 Special Organs of Sense. — The halteres of Diptera contain sensory organs, but their function has not yet been definitely ascertained. pron. Fig. 18. — Gryllus pennsylvanicus. A, Ventral view of thorax; B, dorsal view of thorax, distal portion of pronotum removed; C, lateral view of thorax and abdomen. Cox., C0X.2, Cox-z, First, second and third coxae; Stl., prosternellum; 5/. 2, 5/. 3, meso- and meta-sternum; Pron., pronotum; £0.2, £5.3, meso- and meta-episternum; Em.2, Em.T,, meso- and meta-epimeron; i, 2, 3, etc., abdominal tergites; 1', 2', 3', etc., abdominal sternites; p., peritreme; S., spiracle; sp., supra anal plate; C, cercus; Ovp., ovipositor; pi., pleuron; Sc.2, Sc.3, meso- and meta-scutum; Scl.2, Scl.3, meso- and meta-scutellum; p.scl., postscutellum; W., W.2, wing bases. When deprived of halteres flies cannot maintain their equilibrium in the air. 14 ECONOMIC ENTOMOLOGY ■tr f tb (b) Thorax. — The thorax is composed of three segments — the pro-, meso-, and meiaihorax, each having a pair of legs. The meso- thorax and metathorax bear wings. Each segment is divided into a dorsal part, the notum or tergum, a ventral part, the sternum, and two laterals, the pleura (Fig. 17). Each part is again divided by sutures into sclerites — the notum into prcescutum, scutum, scutellum and post-scutellum, and the pleuron into episternum and cpimeron (Fig. 18). In most hymenopterous insects the first abdom- inal segment — the propodeum or median segment — is fused with the thoracic mass, so that the petiole of such insects is not the first but the second abdom- inal segment. Legs. — Each leg is composed of the following parts: coxa, trochanter, femur, tibia, and tarsus (Fig. 19). The trochanter in certain Hyraenoptera is made of two segments, while the tarsus in most in- sects is composed of several segments, the last bear- ing a pair of claws. In some insects, e.g., the Diptera, three appendages are borne between the claws, in which case the outer pair are termed pulvilli and the middle one the empodium. Wings. — The two pairs of wings are attached to the meso- and the metathorax. They are membran- ous expansions of the body wall with hollow thick- enings along certain lines called veins or nerves. These veins often branch and interlace, and the spaces between the veins are called cells. Much import- ance is attached in classification to the wing and its veins on account of the great variation not only in the orders and families but even in the genera of a family. Structurally the wings of insects may be grouped into three divisions: I. Where the fore and hind wings are of similar texture and more or less fan-like. Under this division fall the Dragon flies, in which both the size and form of the wings are very much alike. Butterflies, wasps, and bees have their hind wings smaller than the fore wings, while some of the Fig. 19. — Leg of a beetle {Calo- ioma caliduni). c, Coxa; c/., claws; /., femur; i., spur; t.^-t.'^, tarsal seg- ments; tb., tibia; tr., trochanter. {After Folsotn.) STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 15 May flies and the males of scale insects have their hind wings very much reduced or entirely wanting. In the flies (Diptera) the hind wings are converted into halteres (balancers). 2. Where the fore wings are either wholly or partially chitinized. Examples of such thickening of the wings occur among the grass- hoppers and crickets, the beetles and the heteropterous bugs. 3. Where the hind and fore wings are strongly reduced or completely atrophied, as in the fleas (Siphonaptera), bird-lice {Mallophaga) and sucking lice {Siphnnculata) . Venation. — It has been found that the system of veins in the different orders of insects is fundamentally alike, being de- rived from the primitive type fairly well seen in some stone- flies and some cockroaches. This fact becomes evident only when a comparison is made of the wings of the more general- ized members of the different orders, as specialization has greatly modified their structure in most genera. Comstock and Needham have shown by a study of the developing wings of nymphs and pupaj that the /'^- 20.--Several stages in the de- "^ , .... . . velopment of the wings of a cabbage butter- principal longitudinal vems m fly. {After Met cer.) the more generahzed orders are formed about tracheae (Fig. 20). In the development of the wing these tracheae grow out into the wing-bud, and later the veins are formed about them. The cross veins, however, as a rule do not arise in this manner, as tracheae are apparently absent. In the course of development specialization has brought about changes in the venation, recognized, first, by the addition of veins through branching of the prin- i6 ECONOMIC ENTOMOLOGY cipal veins as in many Neuropteroids and Orthopteroids; second, by the addition of cross veins; and third, by the reduction of the number of veins §£L Sc2 3dA 2dA IstA Fig. 21. -The hypothetical primitive type of wing venation. Needhatn.) {After Comslock and through coalescence of adjacent veins, or by the disappearance of veins, as in most moths, flies and hymenopters. The chief longitudinal veins are the costa (C), an unbranched vein on or near the front margin; the suhcosta (Sc); the radius (R); the media (M); the cubitus (Cu); and the anal veins (A), typically three but often reduced to one or two. A knowledge of the different types of venation is very important in classifica- tion. The Comstock-Needham system of terminology is adopted in this Classbook, and students should consult the recent work of Professor Comstock — The Wings of Insects — for a full discussion of the general characteristics of the wings of the several orders of insects. Clothing of the Wings. — While the wings of many insects are naked, many are covered with fine setae, hairs, or scales. The coating of scales is the most distinc- tive feature of the wings of the Lepidop- tera. These scales are modified setae, being evaginations of greatly enlarged hypodermal cells. They are provided with ridges, these serving to increase their rigidity and their protec- FiG. 22. — Various forms of scales. A, E, Thysanuran {Machilis); B, beetle {Anthre- nus); C, butterfly (Pieris); D, moth (Limacodes) . STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 1 7 tive value (Fig. 22). In addition, the beautiful colors are due to the scales, and are produced (i) by the pigments present, (2) by the reflection, refraction or diffraction of light, or (3) by a combination of these causes. Scent glands, called aiidroconia, are associated with the scales, mainly on the wings of males. (c) Abdomen. — The abdominal segments show a greater uniformity in form than do the thoracic segments, owing to the fact that the former are not speciahzed for the bearing of legs and wings. This uniformity is not merely external but extends to some of the internal organs, notably the muscular, respiratory and nervous systems. A greater differentiation and consequent difference from the other segments is usually found in the terminal segments which are modified to bear the genitalia and cerci, in the first segment in the Hymenoptera which has united closely with the thoracic mass, and in the petiole of the same insects which is greatly reduced in diameter and often nodulated (ants). Typically the abdomen consists of ten segments, but in some Orthoptera eleven have been found and twelve in a few embryos. In the adult insect it is often difficult to distinguish ten abdominal segments owing to the fusion or disappearance of certain of the segments, to the modification which the terminal segments undergo, or to the telescoping of these last within the other segments. Each segment is made up of a dorsal Sclerite, the tergum, a ventral sclerite, the sternum, and a pair of pleural membranes connecting the two. The first seven or eight abdominal segments usually bear a pair of spiracles each. Typically the anus opens in the tenth or last segment and the reproductive system between the eighth and ninth. Appendages of the Abdomen. — In the embryo the abdominal seg- ments bear paired appendages which are homodynamous with the legs and mouth-parts. These usually for the most part disappear on hatch- ing, but they persist as prolegs during the larval Ufe of the Lepid- optera, Tenthredinidae and Mecoptera; in certain Thysanurans they persist as rudimentary abdominal appendages throughout the life of the insect. The cerci which are present in most of the more generalized orders and in the thysanuriform larvae are usually the appendages of the tenth abdominal segment. The gonapophyses or plates of the genitalia are the appendages of the seventh, eighth and ninth segments and are known respectively as 1 8 ECONOMIC ENTOMOLOGY the ventral, inner and dorsal plates. The inner pair usually forms the ovipositor or the intromittent organ, and the outer pairs may form a sheath or claspers. The Genitalia. — A knowledge of the genitalia is of importance to the taxonomist because in certain families the separation of species is based largely on these structures. It is also of importance to the economic entomologist because it enables him to understand the method of egg deposition in injurious and beneficial insects and the poisonous action in certain forms in which the ovipositor has been modified to form a sting. Fig. 23. — Abdomen of female house-fly, showing extended ovipositor, a., Anus; c, cercus; d.p., dorsal plates; v. p., ventral plate. There is no true ovipositor in the Neuropteroida, Coleoptera, Lepidoptera or Diptera, the vagina opening directly to the exterior (Fig. 23). In some of these insects, however, a whip-Hke or tubular pseudo-ovipositor is formed by the last few segments of the abdomen {e.g.y Cerambyx, Cecidomyia, Musca). A true ovipositor is developed in the Thysanura, Orthopteroida, Hemiptera and Hymenbptera (Fig. 24). In the Orthoptera the gona- pophyses are used for making holes in the ground or shts in stems for the reception of the eggs. In the Hymenoptera there are various peculiar modifications of the ovipositor: Megarhyssa, one of the larger ichneumon flies, uses its long ovipositor as a drill, forcing it, in spite of its extreme slenderness, up to the hilt in the trunk of hardwood trees in order to deposit its eggs in the burrows of the horn-tail borer STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 19 {Tremex columba); the saw flies have the inner plates united to form the egg channel, the upper plates form a sheath, while the lower have serrate edges and are wielded Hke a saw, making slits in leaf or stem for the deposition of the eggs. In the stinging hymenoptera the ovipositor is modified to form a sting; the upper valves of the honey bee are soft, forming a pair of palpi, the inner lobes form a sheath, and the ventral lobes are represented by a pair of barbed darts. The poison is of two kinds, one alkaline the other acid, and is secreted by glands within the abdomen. INTERNAL ANATOMY The internal anatomy of an insect may be discussed under the following heads: {a) muscular system; {b) respiratory system; (f) circulatory system; {d) intestinal or digestive system; {e) nervous system; (/) reproductive system (Fig. 25). (a) Muscular System. — The muscular system xif insects is well developed. The muscles are attached to the inner surfaces of the exoskeleton. In the abdomen the arrangement of th.e muscles is the same in each segment, except at the extremity where special mus- apparatus of honey bee. ag., ^ . . -^ ^ . Accessory gland; p., palpus; Cles exist for moving the ovipositor, the pg., poison gland; r.. reser- cerci or other terminal organs. In the ^ J^ ;'" ^^"'^- ^'^^^''' ^"''' sternum of each abdominal segment there are one or two sets of longitudinal muscles on each side of the nerve chain. These are the longitudinal sternals or ventral recti (Fig. 26). In the tergum also similar sets of muscles occur on each side of the dorsal vessel; these are the longitudinal tergals or dorsal recti. Between these longitudinal muscles and the integument are numerous oW/g«e and trans- verse muscles, and these, with the longitudinal muscles, bring about the various turning, wriggling or telescoping movements of the abdomen. In each abdominal segment there are also two muscles which pass from the tergum to the sternum. These are the tergo-sternals which Fig. 24. — Sting and poison 20 ECONOMIC ENTOMOLOGY bring about the contraction and expansion of the abdomen necessary for respiration. In the thorax of larval insects and of the wingless forms the arrange- ment of muscles follows the same general plan as in the abdomen, but the presence of the leg muscles makes it more complicated (Fig. 27). In the winged insects, however, this primitive arrangement cannot be readily recognized owing to the presence of large wing muscles and also to the fact that the thoracic segments are very often fused together. The muscles which move the head originate in the prothorax and are inserted into the base of the head. Within the head are muscles Fig. 25. — Internal organs of the cricket {Gryllus pennsylvanicus). AN., Anten- nal nerve; Oes., oesophagus; Br., brain; T., teutorium; Ao., aorta; S., suspensorium of ovary; H., heart; Ov., right ovary; Col., colon; R., rectum; A., anus; MT., Mal- pighian tubules; Od., oviduct; Op., ovipositor; BC, bursa copulatrix (copulatory pouch); Vag., vagina; RS., receptaculum seminalis; Mes., mesenteron; VC, con- nectives of ventral nerve chain; VG., ganglia of ventral nerve chain; S.GL, salivary glands; Lb.N., labial nerve; SG., subcesophageal ganglion; Md.N., mandibular nerve; SD., salivary duct; HP., hypopharynx; P., pharynx; Mx.N., maxillary nerve; LN., labial nerve; ON., optic nerve; C, crop; P., proventriculus; GC., gastric cseca. for the control of the mouth-parts and antennae. In the mandibulate insects the muscles which move the mandibles occupy the greater part of the head cavity. Mention should also be made of the alary muscles of the heart, the circular and longitudinal muscles of the digestive canal, and the spiracular muscles which bring about the closure of the spiracles during respiration. A muscle consists of a bundle of long fibres, each with several nuclei and a sheath, the sarcolemma. In most cases the fibres present a striated appearance due to the presence of alternate light and dark bands. STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 21 el. tridt.. v.rma/. vrmin. Fig. 26. — Ventral surface of larva of Sphida obliqua, showing arrangement of parts. AN., Antennal nerve; CL., clypeo-labral nerve; Al.c, alimentary canal- LG., lateral ganglion; /;-., tracheal trunk; tr.lat., tergo-sternal muscles; v.r.maj', v.r.min., ventral longitudinal muscles; S.lig., suspensorium of testes; Test., testis- V.d., vas deferens; Sp., spiracle; T., thoracic ganglia; /, II, III. etc. abdominal ganglia; o.l., oj.cr.ing 'nto leg; tr.r., transverse nerve; BB., brain. 2 2 ECONOMIC ENTOMOLOGY (b) Respiratory System. — The exchange of gases in respiration is effected by means of a system of small tubes called trachea which extend inward from the surface and branch to all parts of the body. The external openings, called spiracles, are situated on the sides of the thoracic and abdominal segments (Fig. 28). From each spiracle a short tube runs inward and connects with the trunk tube running along the side of the body. There are thus two main or trunk tracheal tubes, one on each side of the body. Each gives off three large branches to each segment, the upper, the middle, and the lower. Each of these vf/.f. Ext Tib, Fl.T/b. TlTjUFiTars Ext.Tarij Fig. 27. — Muscles of hind leg of Gryllus pennsylvanicus. Ext.F., Extensor of femur; Ext.Tib., extensor of tibia; Exl.Tar.i, extensor of first tarsal joint; Ext.Tar.2, extensor of second tarsal joint; Exl.Tar.3, extensor of third tarsal joint; Fl.Tat.i, flexor of first tarsal joint; Fl.Tar.2, flexor of third tarsal joint; PLC, flexor of claws; Ext.C, extensor of claws; Fl.F., flexor of femur; Fl.Tib., flexor of tibia. branches subdivides frequently so that every portion of the segment is entered. Moreover, these fine tubes anastomose to form a deli- cate network, and allow a continuous circulation of air to take place. In many insects, in addition, are large sac-like dilatations of the tracheae which serve as air reservoirs. Tracheae have a striated appearance due to the thickening of the chitinous wall into a compact elastic spiral, thus preventing the collapse of the tubes. Special respiratory devices are seen in aquatic insects. Nymphs of May-flies and Damsel-flies have lamellate tracheal-gills, STRUCTURE, GROWTH AND ECONOMICS OF INSECTS nymphs of Stone-flies and Caddice- flies have filiform or cylindric tra- cheal-gills, larvas of Culex, Corethra, Simiilimn and Chironomus have blood-gills, while nymphs of Dragon FHes have internal tracheal-gills . Tracheal gills are outgrowths of the body wall with fine tracheal tubes, in which there occurs during res- piration an exchange of gases be- tween the air in the tubes and the water. They are usually external but in the nymphs of Dragon Flies they are internal, being arranged in rows on the inner walls of a gill chamber in the posterior portion of the alimentary canal. Blood-gills are outgrowths of the body wall in which the blood flows. The exchange of gases in respira- tion occurs between the blood in- side and the water outside. Structurally a trachea consists of a chitinous wall or intima as a lining membrane spirally thickened at regular intervals by elastic threads called tcBnidia, and a cellu- lar wall of hypodermal cells, the pavement epithelium . (c) Circulatory System. — While there is a blood circulation in insects the only blood vessel is a dorsal tube lying just beneath the notum. The heart or posterior portion of the dorsal tube contains a number Fig. 28. — Respiratory system of the larva of the budmoth (Tmetocera ocel- lana) . (Insect opened along the median of ventricles or chambers, each with dorsal line.) C, tracheal commissure; a lateral valve which allows the ^- ^°"'^^ ^'■^"'=^= ^- supplying heart; blood to flow in but not out. There v., ventral branch; F5., visceral branch. 24 ECONOMIC ENTOMOLOGY are also valves between the chambers so that when the latter con- tract the blood is forced forward. The blood on leaving the ventri- cles passes into the aortic portion of the dorsal tube, toward the head, and thence flows into the body cavity bathing all the organs. The blood is usually colorless and consists of two portions — the watery serum and the white blood corpuscles. Fat-bodies. — These are masses of fat-cells occupying a large part of the cavity of the body, and lying between the organs. At first the fat- cells are large and spherical, but they lose their structure to a large extent through breaking down. They contain nourishing albuminoid matter, besides uric acid and urates. Their exact function is not Fig. 28a. — Apparatus for closing the spiracular tracheae in a beetle (Lucanus). A, Trachea opened; B, closed; b., bow; bd., band; c, external cuticula; I., lever; m., muscle; s., spiracle; /., trachea. {After Judeich and Nitsche.) definitely known. Associated with the fat-bodies in the abdomen of larvae are large yellow cells called cenocytes which, according to Glaser, secrete an oxidizing enzyme. {d) Intestinal or Digestive System. — This system occupies the central portion of the body, and is divided into distinct regions with special functions (Fig. 29) . The food passes from the mouth into the pharynx where it is subjected to the action of saliva secreted by the salivary glands. Thence it passes in the Orthoptera and Coleoptera through the oesophagus into the crop, a folded and membranous pouch, where the action of the sahva is completed. The partially digested food then passes into the gizzard or proventriculus , a muscular enlargement armed with teeth for the purpose of straining the contents before entering the true stomach or ventricuhts, In many caterpillars the food passes STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 25 Fig. 29. — Digestive canal of Gryllus pennsylvaniciis. sd., Salivary duct; Oes., oesophagus; Sg., salivary gland; C, crop; pv., pv.", proventriculus; gc, gastric caeca; m., mesenteron; Mv., valve between two divisions of the mesenteron; gl., digestive glands; il., ilium; u.d., duct of malpighian tubules; ut., malpighian tubules; Col., colon; rt., rectum; An., anus. 26 ECONOMIC ENTOMOLOGY Fig. 30. — Dorsal view of ali- mentary canal of the larva of the budmoth {Tmetocera ocellana). Ph., Pharynx; Oes., oesophagus; SM., suspensory muscles; Tr., vis- ceral tracheal of left side; MT., Malpighian tubules; Mes., mesen- teron; Int., small intestine; In., intestinal nerve; R., rectum. directly into the stomach which is long. Further digestion occurs here through the action of secretions of the c(Bcal tubes, often called the gastric cceca, which con- sist of glandular pouches emptying into the anterior end of the stomach. Most of the digested food is here absorbed and passes into the circulation. Pos- terior to the stomach is the intestine which consists of three parts — ileum, colon, and rectum. Into the ileum open the Malpighian tubes which are excretory in function, similar to the kidneys of higher animals. The undigested portions of food are expelled through the rectum and anus. Some variations may be noted. The oesophagus is long in those insects that suck their food, and short in herbivo- rous forms. In sucking insects the giz- zard may be absent, and the crop is often a side pocket of the oesophagus (Fig. 30). Structurally, the wall of the alimen- tary canal consists of: 1. An epithelial layer of cells which secrete the intima or lining layer. 2. The delicate basement membrane. 3. Circular muscles. 4. Longitudinal muscles, which aid in constricting and enlarging the canal (Fig. 31)- From an embryological point of view the alimentary tract consists of three primary regions: 1. The Stomodceum, embracing the fore part as far as the stomach. 2. The Mesenteron, or mid-intestine embracing the stomach, and STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 27 Fig. 31. — Sections through the proventriculus of Gryllus pennsylvanicus. (All greatly enlarged.) i. Longitudinal section through the median denticles. 2. Transverse section passing through two folds of the anterior division of the proven- triculus. 3. Surface view of a portion of one of the dental folds showing the chi- tinous partition and four of the transverse rows of teeth. 4. Transverse section of proventriculus passing through the median denticles. 5. Transverse section of fold cut in the region of the lateral denticles. 6. Lateral view of two adjacent inner barbated lobes, hr., Bristles of anterior division of proventriculus; ch.p., chitinous partition between dental folds; cm., circular compressing muscles; c.v., cardiac valve; ep., epithelium; i.bl., inner barbated lobes; in., intima; l.d., lateral denticle; l.t., lateral tooth; m.d., median denticles; m.t., median tooth; o.b.L, outer barbated lobes; r.m., relaxing muscle. 28 ECONOMIC ENTOMOLOGY 3. The Proctodeum, embracing the portion posterior to the stomach. The stomodoeum and proctodoeum are ectodermal in origin while the mesenteron is probably entodermal. (e) Nervous System.— The nervous system of insects consists essentially of a series of ganglia joined by a double nerve-cord lying along the ventral surface of the body. Each primitive segment had a double ganglion, but in most insects fusion of ganglia occurs in the head, the thorax, the anterior and the posterior portions of the abdomen. Great variations occur even in the same order. The largest ganglion is in the head, and is the result of the fusion of three pairs. It forms the brain or supra- (esophageal ganglion, lying above the oesophagus. There is also another large ganglion, the suh-cesophageal, lying below the oesophagus, and connected with the brain by a double nerve-cord about the oesophagus, the oesophageal nerve collar or commissure. It also repre- sents the fusion of three pairs of ganglia. From the brain nerves are given off to the antennae, eyes, and labrum. The sub- oesophageal ganglion controls the mouth-parts. From the ganglia in the thorax and abdomen nerves supply the various segments and control their movements and activities (Fig. 26). In addition there is the Sympathetic nerve system which mainly lies along the dorsal hne of the alimentary canal. It consists of a recurrent nerve arising from a, frontal ganglion and ending in a stomachic ganglion. Two pairs of lateral ganglia are connected with the recurrent nerve and supply nerves to the dorsal vessel and the tracheae of the head. A ventral system lies in the main nerve cord and activates the spiracles. Nerve-cord and Ganglia. — The nerve-cord consists of an axis-cylinder of fibrillae and a sheath. It is concerned with the transmission of impulses and stimuli. The ganglion is a centre for the regulation of nutrition. It consists of a dense cortical layer of gangUonic cells with large nuclei, a clear medulla from which nerve fibrillae originate, and a nerve sheath. (/) Reproductive System. — In all insects the sexes are distinct. The sexual organs are situated in the abdomen and consist in the female of a pair of ovaries and a pair of oviducts opening into the vagina and frequently externally by an ovipositor, and in the male of a pair of testes and a pair of seminal ducts {vasa deferentia) opening into the ejaculatory duct and externally by an intromittent organ. The external opening lies between the eighth and ninth segments of the ab- STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 29 domen— never in the last. In most insects there is in the female a seminal receptacle, a dorsal pouch of the vagina, and in the male a seminal vesicle, a dilated portion of the vas deferens. The ova are formed in the ovarian tubes in different stages of growth, the largest and oldest being nearest the oviduct. The spermatozoa arise in the -susp. -5usp. ov. ubr -~ed. sp.c. -int. Fig. 32. Fig. 33. Fig. 32. — Male reproductive organs of Gryllus pennsylvanicus. T., Testis; Susp., suspensorium of testis; vd., vas deferens; ubr., u.maj., accessory glands on surface of seminal vesicle; ed., ejaculatory duct; sp.c, spermatophore cup; int., intromittent organ or penis. Fig. 33. — Female reproductive organs of Gryllus pennsylvanicus. Susp., Sus- pensorium of ovaries; O., ovaries; ov., ovarian eggs; od., oviduct; C cercus; r.s., seminal receptacle; d., duct of seminal receptacle; vag., vagina; be, copulatory pouch; Ovp., ovipositor. follicles of the testes. There are also usually accessory glands which secrete mucus that envelopes the spermatozoa and ova (Figs. 32 and 33)- Parthenogenesis, or reproduction without fertilization, occurs in many insects — in aphids, Cynips, Lasius (Ant), and some Coccids. 30 ECONOMIC ENTOMOLOGY Several generations of females only which bring forth living young may occur, but at intervals males appear and fertihzed eggs are laid. In some species of the Cecidomyiidae the young are produced by larvae. Such a method is called pcsdo genesis. After several genera- tions, however, the last larvas pupate and form normal male and female flies. Examples are Tanytarsus dissimilis and Miastor americana (Fig. 2>2,a). Another method of asexual reproduction, called polyembryony occurs in certain parasitic insects, e.g., Polygnotus, belonging to the Hymenoptera. Each egg produces many embryos, instead of one, which develop into as many adult insects of the same sex. Pig. 33a. — Young pasdogenetic larvae of Miastor in the body of the mother larva. Greatly enlarged. {After Pagenstecher from Folsom.) The Development of Insects All insects that reach maturity pass through two distinct stages of development — the embryonic changes within the egg, and the changes after leaving the egg until the adult condition is reached. The growth of the embryo within the egg progresses from the seg- mentation of the ovum to the formation of the blastoderm with its ventral plate and germinal groove, and the gradual growth of the ectoderm, mesoderm and entoderm, from which layers the various organs of the body arise. (a) Embryology. — The egg or ovum is a single cell containing — (i) The nucleus or germinal vesicle. (2) The yolk, or nutritive material. (3) The cytoplasm. (4) The cell wall or vitelHne membrane. (5) The egg shell or chorion. (6) The micropyle or opening in the chorion to admit the spermatoza (Fig. 34). When the sperm nucleus unites with the nucleus of the egg, and forms a segmentation nucleus, fertilization is accomplished. By division of the segmentation nucleus a large number of nuclei are formed many migrating outward toward the margin of the egg. There a layer of cells internal to the yolk membrane called the blasto- STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 31 derm is finally produced. This stage of the embryo is known as the blastula. ^-Ast. Pig. 34. — F'ormation of the blastoderm and the germ band. Fk., Cleavage nuclei; Bl., blastoderm; Kst., germ band. {After Escherich.) , The blastoderm thickens by cell division in one region forming the primitive streak or germ band which presents in surface view an oval or elongated area along the ventral face of the egg. Soon a groove Fig. 35. — Diagrammatic sagittal sections to illustrate invagination of germ band in Calopleryx. a., Anterior pole; ac , amnion cavity; am., amnion; b., blastoderm; d., dorsal; g., germ band; h., head end of germ band; p., posterior pole; s., serosa; v., ventral; y., yolk. {Folsom after Brandt.) appears in the centre of the germ band due to invagination of the blastoderm. The lips of the groove close over the invaginated portion, producing an outer \a.yer, the ectoderm or edoblast and the.inner\a,yer, 32 ECONOMIC ENTOMOLOGY the endoblast (meso-entoderm) . This stage of the embryo is known as the gastrula. Meanwhile the blastoderm is folding over the germ band from either side, producing an inner membrane — the amnion, and an outer membrane — the serosa (Fig. 35). Two types of germ bands may be noted. The overgrown type retains its original position (Fig. 36), and the blastoderm folds over the germ band from either side forming the two layers amnion and serosa. In the invaginated type, seen in aphids and Odonata (Fig. 37), the germ band invaginates into the egg so that its ventral surface faces the dorsal surface of the egg. At a later stage the embryo turns and regains its original position. The germ band shows early signs of segmentation, beginning first at the anterior end. An in- vagination of the ectoderm near the anterior end forms the stomo- doeum or fore gut, and a similar posterior invagination forms the proctodceum or hind gut. The segmentation shows about 21 seg- ments, 6-7 to the head, 3 to the thorax, and 11-12 to the abdo- men. On each segment except the first and last a pair of tiny limbs (buds) are seen. Soon the germ band widens and closes over the yolk to form the dorsal waU. Before dorsal closure occurs the beginnings of the nerve-cord form in the median groove. This primitive nerve-cord is double, and a pair of swellings in each segment develop into the ganglia of the ventral system. The tracheas arise as invaginations of the ectoderm. The entoderm arises from the endoblast, the inner embryonic layer, as two cell masses situated at either end of the embryo. These masses grow backward and forward respectively, and unite to form the mid- gut {mesenteron) . The rest of the inner layer forms the mesoderm from which arises Pig. 36. — Formation of the embryonic membranes — overgrown type. Am., am- nion; Ect., ectoderm; Enl., entoderm; Ser., serosa. {After Korschelt and H eider.) STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 33 the blood system, muscles, reproductive organs, fat-body, etc. The division of the mesoderm into two layers produces paired cavities in each segment — the ccelomic pouches (Fig. 37). {b) Metamorphosis. — The various changes that occur after the hatching of the egg are comprised under the term metamorphosis. After the escape of the embryo from the egg the development may be (i) holo- metabolic, i.e., with complete metamorpho- sis, the insect passing through two distinct phases, larva and pupa, before assuming the adult form; (2) heterometaboUc, i.e., with incomplete metamorphosis, without a dis- tinct pupal stage, the larva being like the adult but without wings or mature repro- ductive organs; (3) ametabolic, i.e., without metamorphosis, the young being Hke the adult. Insects belonging to the orders Neuroptera, Mecoptera, Trichoptera, Lepidoptera, Coleoptera, Diptera, Sipho- naptera, and Hymenoptera are holome- tabolic; the Orthoptera, Platyptera, Ple- coptera, Odonata, Ephemerida, Thysan- optera, Homoptera and Hemiptera are heterometabolic; and the Thysanurans and Collembolans are ametabohc. Most insects are oviparous, but some like cer- tain scale insects and Sarcophagidae are larviparous. Larval Stage. — In general two types of larvae are recognized : the thysanuriform and the eruciform. The former type is considered quite generalized and primitive in form, and is common among the hetero- metabola. The body is flattened, the legs and antennae are long, the caudal cerci are well-developed, and the mouth-parts are mandibulate. Pig. 37. — Embryo of jEcan- thus, ventral aspect, a, An- tenna; a.^-a.^, abdominal ap- pendages; e., end of abdomen; I., labrum; li., left fundament of labium; Ip., labial palpus; L^-l.^, thoraciclegs; w., mandi- ble; tnp., maxillary palpus; mx., maxilla; p., procephalic lobe; pr., proctodoeum. {From Fol- som after Ayers.) 34 ECONOMIC ENTOMOLOGY The cruciform type prevails among the holometabola. The body is cyHndrical, and the legs, antennae and cerci are much reduced. Many transitional forms, however, occur, and it is believed that the cruciform type has been developed from the thysanuriform. Ecdysis or Moulting.— AW larvae shed their outer skin (cuticula), at intervals to allow for growth. The number of moults varies in different insects, but is constant for the same species under the same conditions. In the Lepidoptera the larva is known as a caterpillar, and is char- acterized by the possession of three pairs of true legs, and usually Pig. 38. — Types of larvae, a. Grub of asparagus beetle; b, cutworm; c, cabbage root maggot; d, fall canker worm;'e, maggot of honey bee; /, spring canker worm; g, false caterpillar of saw fly; h — a, b, c, nymphs of locust; i — a, b, c, d, e, nymphs of squash bug. {After various authors.) five pairs of prolegs on the abdominal segments. In the Diptera and Hymenoptera the larva is a maggot, characterized by the absence of legs. In the group of Saw-flies of the Hymenoptera, however, the larvae are caterpillar-like, possessing three pairs of true legs and often seven or more pairs of prolegs. In the Coleoptera the larva is termed a gruh, and has usually but three pairs of legs (Fig. 38). Classification of Larvae. — Escherich classifies larva; as follows: Primary Larva. — Larva; like the adult, and without provisional larval organs — Thysanura, Mallophaga, PedicuUda, Orthoptera, Isoptera, Corrodcntia. STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 35 Secondary Larva. — ^Larvae like the adult, and with a few provisional larval organs — Ephemerida, Plecoptera, Cicadidcc, Odonata, Coccidce. Tertiary Larva. — Larvae unlike the adult and with numerous provisional larval organs — Lcpidoptera, Dlptera, Coleoptera, Hymcnoplera, etc. ■ Classificalion of Tertiary Larva. A. Larvffi without prolegs. B. Larvae with well-formed sternum. C. Larvae more or less strongly chitinized; thorax or at least the prothorax differing from the other segments quite noticeably, large or more strongly chitinized, or otherwise sculptured; head generally with lateral eye points. Examples: Rhaphidians Ant-lions, Carabida, Dytiscida, Silphida, Coccinellida, Elalerida, Chrysomelida. CC. Larvae weakly chitinized, soft skinned, and mostly whitish, but with chitinized dark head; thorax differing but little from the other segments. Examples: White Grubs, Stag Beetles, Dung Beetles. BB. Larvae with poorly developed or rudimentary sternum. Examples: Many Cerambycids, Sirex. BBB. Larvae with sternum whoUy atrophied or undeveloped. C. Larvae with a head-capsule and typically formed mouth-parts. Examples: Bark Beetles, Snout Beetles, Bees, Wasps, Ants, Ichneumons, Midges. CC. Larvae without a head-capsule or well-formed mouth-parts. Examples: Most Diptera. AA. Larvae with prolegs. B. Larvae usually with five pairs of prolegs. Butterflies and Moths. BB. Larvae with more than five pairs of prolegs. Sawflies. Provisional Larval Organs. — Provisional larval organs are those which belong to the larva and not to the imago. According to Escher- ich such organs represent adaptations for special functions, so that the more numerous these organs are the greater the difference in mode of life and in appearance between the larva and imago. As the imago is older phylogenetically than the larva the larval organs have arisen in a secondary manner. "Secondary" larvae possess numerous imaginal characters, so that the form of the imago remains more or less evident. In "tertiary" larval forms the characters of the imago are so repressed by those of the larva that a new form unlike the imago results. Larval organization distinct from that of the imago may be observed: (i) in the amount of chitinization, the color and the armature of hairs, bristles, spines of the skin; (2) in the number of glands; (3) in the form 36 ECONOMIC ENTOMOLOGY and segmentation of the body; (4) in the development of feelers and mouth-parts, (5) in the number and development of organs of locomotion and (6) in the alimentary, tracheal and nervous systems. Examples can be readily found to illustrate the differences outlined above. Pupal Stage. — After a short period of rest the full-grown larva of holometabolic forms changes to a pupa within a pupal skin. Usually the outer skin is shed, but sometimes, as in the Diptera, the outer skin becomes a puparium. During the pupal stage not only are all the Fig. 39. — Types of pupae, i. Asparagus beetle (free); 2, puparium of cabbage root maggot (coarctate); 3, bud moth (obtect); 4, tobacco sphinx (obtect); 5, male of maple scale (free). external organs of the adult insect formed, but even the internal organs undergo profound changes. The organs break down and reform, and the structures are adapted to the new creature with its new mode of life. In most insects the pupa is quiescent but it is quite active in the Culicidae and other families. There is but little difference, except the presence of rudimentary wings, between the larval and pupal stages of the insects belonging to the Hemiptera and the Orthoptera. Three types of pupae are recognized (Fig. 39): (i) ohtect, where the appendages and body are closely united, as in Lepidoptera and some Coleoptera; (2) free, where the appendages are free, as in Neuroptera, STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 37 Trichoptera, Coleoptera, Hymenoptera and Nematoceran Dipera; and (3) coarctate in which the entire pupa is surrounded with a hardened skin, and the appendages are not outwardly visible, e.g., higher Diptera (Muscids, etc). Pupas are protected in different ways: (i) in puparia, (2) in earthen cells in the ground, (3) in a rude cocoon in wood or earth, (4) in silken cocoons, (5): in folded leaves, (6) as chrysalids. Examples of the above types are everywhere about us. Internal Changes. — ^In the heterometahola the internal changes are as direct as the external changes. In the holometabola, however, some Fig. 40. — Stages in the hypermetamorphosis of Epicauta. A, Triungulin; B, carabidoid stage of second larva; C, ultimate stagejof second larva; D, coarctate larva; E, pupa; F, imago. E is species cinerea; the others are vitlata. All enlarged except F. {After Riley, from Trans. St. Louis Acad. Science.) of the larval organs are reconstructed into imaginal or adult tissues. The imaginal organs arise from embryonal tissues (the imaginal buds) which for the most part remain practically dormant in the larval stage; in the pupal stage the purely larval organs disappear and the imaginal organs continue their development. Histolysis is the term used to ex- press the destruction of larval tissue by leucocytes, and histogenesis for the construction of imaginal tissues. Imaginal Buds.—Th.e reproductive organs, the dorsal vessel, and the nervous system gradually mature, but many of the organs develop 38 ECONOMIC ENTOMOLOGY from "buds" in the larva. In the caterpillar, for example, from the inner skin or hypodermis arise buds which develop into the wings and legs of the butterfly. In a midge or fly the head with the eyes, feelers, and jaws, are developed by an inpushing of the skin. The food- canal, glands, and air-tubes of a moth or a bee arise from imaginal buds. Imago or Adult Stage. — The pupa transforms into the imago or adult insect. On the splitting of the pupal case the full-grown perfect insect emerges. (c) Hypermetamorphosis. — With some insects more than two intermediate stages may be noted in metamorphosis. In Meloe the young larva {triunguUn) is thysanuriform; later it resembles a lamel- licorn larva, being cyHndrical, fleshy, and less active (the scaraboeidoid stage), then a pseudo-pupa (the coarctate stage), and later a legless cruciform larva. In Epicauta also triungulate, carabidoid, scara- boeidoid and coarctate or pseudo-pupa stages occur (Fig. 40). In Platygaster, a proctotrypid, the following supplementary larval stages are observed: (i) the cyclops, (2) the oval, and (3) the elliptical. Losses Due to Insects While everyone will acknowledge the fact that damage is done by insects, the enormity of the losses is not generally recognized. How- ever, fairly reliable data covering such losses for several decades in the United States are available in State and Federal records. Every person admits large losses due to such pests as Potato Beetle, Codling Moth, San Jose Scale, Tent-caterpillar, Cattle Horn Fly, and Grasshoppers, but later pages will show many other injurious forms that remain practically unobserved by the average person, on account" of their small size, or their underground or boring habits. The damage they do is often attributed to other causes, and frequently reports are unreliable, unless corroborated by competent observers. The following estimate is based on statistics prepared by experts and published in the Year Book, U. S. Department of Agriculture. The loss on farm products, such as cereals, hay and forage, cotton, to- bacco, truck crops, sugars, fruits, farm forests, miscellaneous crops and animal products, valued at 8370 millions of dollars in 1909, is greater than 10 per cent, for there is a loss of 972 millions, not includ- STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 39 ing those in connection with natural forests and forest products, and products in storage, which would make a probable total loss of over one billion dollars. The losses are estimated at $1,182,000,000 for 1915, and $1,400,000,000 for 1917 (J. Ec. Ent., Feb., 1918). Estimates of the losses inflicted by insect pests on the farm products of Canada are mainly based on similar ones for the United States. At the present time it is difficult to form a reliable estimate of average annual losses due to insects from Canadian records. In some of the older provinces fairly complete records covering a series of years are available, but in the newer provinces the records are incomplete. Estimates have been made of the losses from some of the more serious pests that occasionally cause great damage, such as the Hessian Fly and the Pea Weevil. In Ontario the loss from the Hessian Fly in each of the years 1900 and 1901 was about two and one-half million dollars, and from the Pea Weevil in 1902 over two millions. If, however, the percentage loss in the United States, viz., 10 per cent, be taken as a fair basis for insect loss in Canada it can be readily reckoned that the total loss every year in that country exceeds 100 milUons of dollars. Beneficial Insects While the damage done by insects is enormous it must not be sup- posed that all insects are injurious. As a matter of fact there are more insects that are either beneficial or non-injurious than there are in- jurious forms. Man owes much to the beneficial insects for their good service in keeping the injurious forms in check. The fact that most plants with colored flowers are largely dependent upon the visits of insects for their fertilization and the setting of their fruit should make it quite evident that insects play a most important part in the economy of nature, and are no mean things after all. Let one reflect for a moment on the loss to the world if the blossoms of apple, plum, peach, grape, strawberry and raspberry among fruits were not fertihzed by bees and wasps; if the clovers were not visited by bees, and if the hundreds of beautiful wild flowers of the fields and meadows were allowed to die without setting seeds. In addition, one should not forget the part played by scavenger and carrion insects that feed upon dead and decaying organic matter. They help to make our surroundings purer and cleaner. Besides, 40 ECONOMIC ENTOMOLOGY "insects constitute the most important portion of the food of adult fresh water fishes, furnishing 40 per cent, of their food," according to Dr. Forbes, of IlUnois. They also furnish food for most of our birds, and this food may consist of many noxious forms. There are also many insects that are decidedly beneficial, inas- much as they prey upon injurious forms or are parasitic upon them. At the present time a great experiment is being conducted in Massa- chusetts for the suppression of the gypsy and brown-tail moths by the importation of certain parasitic insects from Europe and Japan (see Part IV). From an economic point of view it is important for us to know the beneficial forms so that we may not unwittingly destroy them. Few persons, perhaps, fully recognize the valuable work done by the modest lady-bird beetles in keeping plant-Hce within bounds. Without their intervention it is quite probable that most plants would die from the attacks of the fast reproducing plant-lice. Ground-beetles are also important agents in the destruction of injurious larvae, and their value can hardly be estimated. Beneficial insects may, therefore, be classified into: (a) Those that prey, or are parasitic, upon injurious forms {en- tomophagous) such as lady-bird beetles, ground beetles, parasitic diptera and hymenoptera, etc. (b) Those that pollinate plants, such as bees, wasps, moths, etc. {c) Those that play the part of scavengers, feeding upon dead or decaying organic matter, such as carrion beetles, etc. {d) Those that serve as food for fresh-water fishes, birds, etc. {e) Those that secrete or elaborate substances of commercial value to man, such as honey-bee, lac insect, cochineal insect, silk- worm, etc. Berlese divides entomophagous insects into predatory and endopha- goiis. Predatory insects are those which devour other insects and their eggs outside the maternal body; while endophagous insects are those which enter the body or eggs of their victim and destroy them. Some entomophagous insects feed exclusively on one species, while others feed on several species (polyphagous) . From the standpoint of efficiency in the destruction of injurious species Berlese arranges them in the following order : I. Those preying on a single species and having few enemies and aflverse factors, e.g., Novius cardinalis, Prospaltella berlesei, etc. STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 4I 2. Polyphagous endophagous species which are themselves sub- ject to severe competition and meet with many adverse factors, e.g., ScutelUsta cyanea, etc. 3. Predators with special victims, e.g., many lady-birds. 4. Polyphagous predatory species; Calosoma. Entomophagous insects include members of the Coleoptera,Hymen- optera, Diptera, Hemiptera and Neuroptera. The coleopterous mem- bers are the lady-bird beetles, murky ground-beetles, and tiger-beetles. The lady-birds are small, convex, nearly hemispherical beetles, generally red or yellow and spotted. Their antennae or feelers are club-shaped, and their tarsi are apparently three-jointed. They feed upon small insects and the eggs of larger species, and are specially valuable for keeping plant-lice in check. The larvae of lady-birds are quite active and hunt for their prey. Some bear spines, while others are protected by fine white down. Ground-beetles {CarabidcB) are active forms that live on the surface of the ground. They are usually black, but some have bright colors. They hide under stones or boards in the day-time but leave their shelters at night. They destroy large numbers of caterpillars, such as cutworms, canker-worms, tent-caterpillars, and the grubs of curculio. The larvae feed underground on the larvae of leaf-feeding insects. The ground-beetles have thread-like antennae, five-jointed tarsi, and legs fitted for running. Tiger-beetles {Cicindelidce) are carnivorous insects, and are most active in the day time. Their activity, markings, and stealthy habits have given them their common name. In structure they are closely related to the ground-beetles, and like them have thread-like antennae and five-jointed tarsi. The larvae of these beetles live in holes in the ground and prey upon unwary insects. They have large heads, immense jaws, long sprawling legs, and two prominent humps on the back. The Hymenoptera possess several very important beneficial forms, mostly parasites: Ichneumon-flies {I chneumonidce) vary greatly in size, and the females of some species possess a protruding ovipositor. A common ex- ample is Megarhyssa (Thalessa) a very long tailed ichneumon, which bores a hole in wood infested with pigeon Tremex borers and deposits an egg beside the larval Tremex (Fig. 41); other common ichneumons are: 42 ECONOMIC ENTOMOLOGY Tragus, which parasitizes the chrysalids of Papilio; and Ophion, a form with a compressed body, which lives on the Polyphemus moth and yellow-necked caterpillar. The Braconids (Braconidce) are smaller and are also parasitic. The most common genera are Microgaster, whose cocoons are often found on the backs of sphinx and cabbage butterfly larvae; and Aphidius which parasitizes plant-lice. Chalcids or chalets flies iChalcididcB) are minute metallic insects. One species, Pteromalus puparum, is a parasite of the chrysalids of the Fig. 41. — Female of Megarhyssa (Thalessa) ovipositing. cabbage butterfly. Another, Aphelintis, is parasitic on scale insects (see also p. 354). Proctotrypids are very minute parasitic hymenoptera often prey- ing upon the eggs of other insects. Besides these parasitic forms there are predaceous Hymenoptera, such as the mud-wasps, digger-wasps, wood-wasps, etc., that feed their larvae on insects. They fill the brood cells with caterpillars, grass- hoppers, plant-Hce, or grubs of small beetles or flies. Sphecius makes use of cicadas as food for its young. Several families of the Diptera are either parasitic or predaceous. The two best known are the Tachinids and the S>Tphids. Tachinids or tachina flies {TachinidcB) are bristly flies closely related to the ordinary house-flies. They parasitize many kinds of caterpillars STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 43 and sawfly larvae, either by inserting eggs within the bodies of their victims or by allowing the victims to swallow the eggs that are deposited on leaves. Syrphids or flower flies (Syrphidce) lay their eggs in colonies of plant- lice which are devoured by the larvae. They are large, often bee-like in form. The Hemiptera include a few beneficial forms, mostly belonging to the assassin-bug family (Reduviidce). They are predaceous, suck- ing the blood of other insects. Sometimes higher animals, including man, are attacked. The following forms may be noted: Melanolestes picipes is a large black form, and Opskcetus pcrsonatus, or masked bed-bug hunter, is black and over 32 inch long. The Stink Bug Family {Pentatomidce) also furnishes a few beneficial species, although a very large percentage of the species is injurious to plant life. Two common forms are: Podisus spinosus (spined tree bug) destroys potato beetles and currant worms, and Perillus circuni- cinctus which appeared recently in large numbers in potato fields where it de- stroyed potato beetles (Fig. 42). The Damsel Bugs (Nab idee) prey upon leaf-hoppers. The Ambush Bugs (Phymatidce) are also predaceous, destroying large numbers of injurious insects. Among the Neuroptera are some important beneficial forms, known as aphis-lions and ant-lions. The adults of aphis-lions, also called lace-winged flies, are readily recognized by their delicate veined green wings. Their larvae are pre- daceous and destroy large numbers of plant-lice. Their mandibles are very long. The genus Chrysopa is the main one in the family. The adults of Ant-lions {Myrmeleonidce) have "long narrow delicate wings and a slender body." The larvae are very predaceous and possess enormous mandibles. They capture their prey by using pitfalls. Hyper parasitism. — It happens that many of the primary parasites are often infested with parasites which reduce very appreciably the Fig. 42. — Perillus circum- cinclus, an enemy of the Colo- rado potato beetle. 44 ECONOMIC ENTOMOLOGY effectiveness of the primary. Frequently, however, these secondary forms are infested with tertiary parasites. In the control of injurious forms it is evident that primary parasites are beneficial, secondary harmful and tertiary beneficial, on the other hand, when beneficial insects are parasitized the primary are harmful, the secondary beneficial and the tertiary harmful. Insects and Birds When it is known that about two-thirds of the food of our common birds consists of insects, it becomes evident that the agency of birds in the control of insects is of the highest importance. The seasonal diet of the robin, bluebird, catbird, king-bird, flycatchers, chickadee, wren, swallow, woodpecker, cuckoo, night-hawk, warblers, oriole and many other birds has been carefully studied in recent years, with the resulting discovery that insects form in most cases their only food, and only at certain seasons are small fruits eaten. Birds are no doubt of special value to the farmer in nipping incipi- ent scourges in the bud on account of their ability to move rapidly from place to place in search of food, and on account of their varied character and habits. Especially is this true of our winter birds which search every cranny and nook for the hibernating forms of insects at a season when every form destroyed means in most cases the absence of hundreds or thousands of their progeny the following summer. An international treaty between Great Britain and the United States for the protection of migratory birds in the United States and Canada was signed in Washington in August, 191 6. For many years the numbers of such birds had been decreasing to such an extent, through careless and indiscriminate slaughter, that the agricultural and forest crops of the two countries were in danger of suffering serious losses from insect depredations. It was deemed advisable, therefore, in the interests of the two countries to adopt a uniform system of bird protection, such as the treaty provides. The most important provision relates to close seasons, viz: (i) a close season on migratory game birds from March loth to September ist except for maritime shore birds when the close season is from February ist to August 15th; (2) an open season for three and one-half months for wild fowl; and (3) a close season throughout the year on insectivorous birds. structure, growth and economics of insects 45 Inter-relations Between Insects and Plants The idea of inter-relations in Nature was first emphasized by Spren- gel, Darwin and Miiller, and later ecological studies reveal still more clearly how all Nature is linked together into a system, one part de- pendent upon another in an intricate web of life. Disturbances in one portion of the system are followed by disturbances in another. In this chapter reference is made to some of the relations be- tween insects and plants, between insects and birds, and between insects and their parasites. Numerous other relations might be mentioned but these are sufficient to show that a knowledge of these relations is an important part of the equipment of the economic entomologist who would deal successfully with the problems confronting him. In a region undisturbed by man the various parts of the system of Nature have practically reached a state of balance through the ceaseless action for long ages of the "struggle for existence." Plant struggles with plant, animal with animal, and both with the environment. With the advent of man, however, the balance has been disturbed by the clearing of the forests, the cultivation and drainage of the land, the growing of crops, and the introduction of foreign plants and animals, since the new set of conditions will be favorable to the increase in num- bers of certain plants and animals, including insects, and unfavorable to others. This disturbance is often widespread. Favored insects will multiply rapidly on account of the abundant supply of food fur- nished by the cultivated crops, faster at first than their parasitic enemies; and insectivorous animals such as snakes, toads, birds and predaceous insects will be deprived of the necessary shelter and hiding places by the clearing of the land, and become less abundant. On the other hand insects not favored, by the destruction of their food plants under the new conditions, will diminish in numbers, as will also their parasites, both sometimes no doubt to the verge of extinction. If, however, as is sometimes the case, conditions again favor the insect it will multiply very rapidly because the development of the parasite lags behind its host. Moreover, there is always a limit to the increase of the parasite, otherwise it would exterminate its host, and eventually itself. Many examples of inter-relationships among insects in addition 46 ECONOMIC ENTOMOLOGY to that of parasite and host might be given. Certain ants attend certain plant-Hce with the object of feeding upon the nectar excreted— and not of feeding upon the plant-hce as some ignorantly suppose. Forbes has shown that the corn-root plant-louse is actually dependent upon the brown ant, Lasitis niger americanus, for its existence, for its transfer to suitable winter quarters, to suitable weeds in early spring, and j&nally to the corn itself. In bumble-bees' nests one may often find a related bee, Psithyrus, living as a guest and fed by the worker bumble-bees. This guest bee is not content to live quietly in the nest; she often destroys the Bombus queen and gets "the poor workers to rear her young instead of their own brothers and sisters" (Sladen). Ants' nests or formicaries often contain a motley crew of other insects, among which are rove-beetles, pill-beetles, fly larvae, small crickets, thieving ants, and parasites — the majority being thieves and robbers. Again, no satisfactory explanation has yet been given for the preferences many insects exhibit in their feeding habits. As ex- amples, we are at a loss to know why in some districts the wheat midge does more damage to spring wheat than it does to fall wheat; why the Hessian fly injures certain varieties of wheat more than others; why the grape blossom midge injures the early varieties of grapes most; why' the Leconte and Kieffer pears are practically immune from the San Jose scale and the white peach scale; why the Northern Spy apple is not troubled with the woolly aphis; why the Red Dutch cabbages are free from the cabbage root maggot; why the spiny elm caterpillar and the European elm scale prefer the American elm to the imported English elm; why the European elm saw-fly and the elm leaf beetle prefer the European elm to the American; why the forest caterpillar attacks the sugar maple in preference to the soft maple; why the maple scale prefers the soft maple to the sugar maple; why the apple maggot is more injurious to sweet and sub-acid summer varieties than to fall and winter-acid varieties; why the brown mite is seldom seen in quince and apricot; and why the phylloxera is more injurious to the European vine than to the native American species. Long-continued observations show that there are "all grades of association between plants and insects from most casual contact to STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 47 mutual dependence, and that there are grades of fitness on both sides" (Needham, General Biology). Reference has already been made in the section dealing with Beneflcial Insects to the important part played by many insects in the fertilization of plants. To this end many beautiful adaptations occur among plants such as in legumes, iris, milk- weed, yucca, orchids, mints, figworts, honeysuckles, canna, Smyrna fig, etc., but it should be borne in mind that there has been also 'probably much adaptation on the part of the insects. Galls. — Another type of inter-relation is the galls seen on many plants, produced by certain insects belonging to the families Cecido- myiidee, Trypetidce, Aphididce, Psyllidce, Cynipida and Tenthredinidce. Mites (Acarina) also produce galls. Usually an egg is laid within the growing tissue and the larva excites the surrounding tissue to abnormal growth. The transformations occur within the gall, and the adult escapes to make new galls. Galls are of various forms, often characteristic of the insects pro- ducing them. The nutritive cells lying next to the contained larva contain both sugar and starch and appear to function as feeders for both the larva and the growing cells of the gall. Insectivorous Plants. — Certain plants such as the sundew, Venus' fly-trap, pitcher-plant and bladderwort entrap small insects and feed upon them. These plants secrete digestive fluids which convert the tissues of the captured insects into liquid food capable of being absorbed. Diseases of Insects. — Many insects are killed by the action of cer- tain fungi and bacteria. Such diseases are frequently epidemic, and attempts have been made to control insect infestations by the propaga- tion and distribution of artificial cultures. Probably the best known experiment of this nature was carried out by Dr. Snow and Dr. Forbes against the chinch bug in the middle States by the distribution of cultures of the fungus S porotrichum globuliferum. The result was only moderately successful, for it was found that the disease spreads rapidly in moist seasons, but not in dry ones when the chinch bugs are inju- rious. There is no doubt, however, that the fungus is an important factor in lessening the severity of the insect's attacks. In South Africa, Algeria and Argentina the locust has been con- trolled by the introduction of bacterial cultures of Coccohacillus 48 ECONOMIC ENTOMOLOGY acridiorum, but in other regions where the weather conditions are not so favorable this method has not met with success. In the southern States the San Jose scale is often attacked by SphcBrostilbe coccophila, but as a means of control artificial propagation of the disease on a large scale has not been successful. Tent-caterpillars, brown-tail and gipsy moth caterpillars are de- stroyed in large numbers by bacterial disease. Following is a list of the more important entomogenous fungi: Empii$a musccB on flies, E. grylli on crickets, etc. and E. aphidis on plant-lice. Entomophthora aphidis on plant-lice, and E. sphcBro- sperma on many caterpillars. Cordyceps militaris on larvae and pupae of white grubs, wireworms and some lepidopterous forms. Most of the conidial forms of Isaria and Sporotrichmn belong to the ascus genus Cordyceps. Botrytis, Verticillium, Cladosporium, Mgerita and Fusarium attack many kinds of insects, especially scale insects, plant-lice,, white flies, and the chrysalids of moths. Future investigations will probably lead to the better utilization of fungi in the control of many of the most noxious insects. Insects as Carriers of Plant Diseases Flea-beetles by eating holes in the leaves of potato permit the en- trance of the spores of Early Blight {Macros porium solani) with conse- quent partial destruction of the leaves. It has also been shown fairly conclusively that certain aphids and other insects^ act as carriers of Twig Blight {Bacillus amylovorus) of apples and pears, that the beet leaf-hopper {Eutettix tenella) transmits to sugar beets the " Curly Leaf" disease, and it is now believed that the squash bug {Anasa tristis), the striped cucumber beetle {D. vittata), the 12-spotted cu- cumber beetle {D. 12-punctata), the cucumber flea-beetle {Epitrix cucumeris), the melon aphis {Aphis gossypii), and the 12-spotted lady-beetle {Epilachna borealis) frequently inoculate the stems of cucur- bits with the cucurbit wilt {Bacillus tracheiphilus). Again, the punc- tures made by the plum curculio in plum, cherry and peach permit entrance of the spores of the Brown Rot Disease {Sclerotinia fructigena) , ^ Gossard mentions among others Aphis avencE, Empoasca mali, Eccoptogasler rugulosus, and Lygus pratensis. "Any sucking insect can become a carrier, also any insect with the bark-burrowing habit." STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 49 and Ihe greenhouse white fly {Aleyrodcs vapor arionim) often transmits the disease Cladosporiuni fulviim to tomatoes. Tree crickets {QLcanthus) are said to be responsible for the inocula- tion of trees and shrubs with canker, of raspberries with the cane blight, and probably for the production of other diseases. Insects and Disease (Consult Handbook of Medical Entomology by Riley and Johannsen, and Medical and Veterinary Entomology by Herms.) During the last twenty years important discoveries have been made regarding the transmission of certain diseases by arthropods such as the mosquitoes, house-flies, stable-flies, gad-flies, tsetse-flies, fleas, bed-bugs, lice and ticks. Insects and arachnidans cause disease in one or more of the fol- lowing ways: by direct infection, that is by the introduction of a patho- genic organism into the circulation, as in the case of the malarial mosquito, the yellow fever mosquito, the sleeping-sickness flies, horse flies and others; by indirect infection, that is by infecting food, as in the case of the house-fly; by internal parasitism as in the case of warble flies and bots; by external parasitism as in the case of lice, fleas, bed-bugs and ticks ; and by the introduction of poisons as in the case of bees, wasps, kissing bugs and others. Brues and Sheppard have divided the diseases that are carried by insects into three groups: Group A. — Characteristically insect-borne diseases. Group B. — Often insect-borne diseases. Group C. — Possibly insect-borne diseases. Under Group A are included malarial fever, yellow fever, filariasis, sleeping sickness, typhus fever, bubonic plague, African tick-fever, Rocky Mountain spotted fever of man, and Nagana and Texas fever of horses and cattle. Under Group B. are included typhoid fever, cholera, dysentery, diarrhoea, tuberculosis, septicaemia. Under Group C. are included anthrax, rabies, pellagra, hookworm, beriberi, black water and relapsing fever of man; and equine infectious anaemia. 50 ECONOMIC ENTOMOLOGY A nopheles Mosquito and Malaria: Malarial fever and ague were common a generation ago, and our fathers vaguely attributed the disease to the presence of swamps whose numbers have fortunately been greatly reduced by drainage. The story of the discovery of the causal organism and of its life- history in connection with the Anopheles mosquito is one of the in- teresting chapters in modern biological investigation. The organism belongs to the amoeboid Protozoa and was discovered by Laveran, a French army surgeon, in 1880. The part of Anopheles as a second or intermediate host of the malarial organism was worked out later by Doctors Manson and Ross. (A full account of the discovery will be found in Kellogg's "American Insects.") The malarial plasmodium on gaining access to the human body lives within a red blood-corpuscle and thrives at the expense of the haemoglobin. A characteristic excretory product in affected cells is the black granules of melanin. In 48 hours the plasmodium reaches maturity and divides into many spores, termed merozoites, which are set free in the blood. These soon enter new blood-corpuscles and reach maturity in 48 hours as before. This production of spores coin- cides with the characteristic "chill" of ague, and is followed by a fever when the spores enter the blood-corpuscles. As a result of the de- struction of the red blood-cells the patient becomes anamic. Certain of these spores, however, make no attempt to enter new blood-corpuscles and may remain in the blood for an indefinite period. These are the gametes — the micro- and macro-gametes — which, if taken into the stomach of an Anopheles mosquito, will, however, undergo further development. The male or micro-gamete produces a number of whip- like threads or fiagellce, which are capable of uniting with the female or macro-gametes, producing vermicules or ookinetes. These penetrate into the wall of the stomach of the mosquito where they rest as cysts, forming little lumps on the outer surface. These cysts mature in about ten days and burst, liberating large numbers of sporo-blasts into the body cavity, whence they find their way to the salivary glands. When such an affected mosquito bites a human being these spores are injected into the blood and enter the red cor- puscles. It will be seen, therefore, that ordinarily the Anopheles mosquito is the only agency for the transmission of malaria to man (Fig. 43)- STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 5 1 Fig. 43. — Life history of malaria parasite, Plasmodium prcecox. i. Sporozoite, introduced by mosquito into human blood; the sporozoite becomes a schizont. 2. Young schizont, ^hich enters a red blood corpuscle. 3. Young schizont in a red blood corpuscle. 4. Full-grown schizont, containing numerous granules of melanin. 5. Nuclear division preparatory to sporulation. 6. Spores, or merozoites, derived from a single mother-cell. 7. Young macrogamete (female), derived from a mero- zoite and situated in a red blood corpuscle. 7a. Young microgametocyte (male) derived from a merozoite. 8. Full-grown macrogamete. 80. Full-grown micro- gametocyte. In stages 8 and 8a the parasite is taken into the stomach of a mos- quito; or else remains in the human blood. 9. Mature macrogamete, capable of fertilization; the round black extruded object may probably be termed a "polar 52 ECONOMIC ENTOMOLOGY Stegomyia Mosquito and Yellow Fever: The demonstration of the causal relation between the Stegomyia mosquito and yellow fever is another interesting story, and was worked out mainly by Major Walter Reed of the U. S. Army Medical Service in Cuba in 1900 and 1901. In his experimental camp Major Reed and his associates proved that yellow fever could not be transmitted by contact with yellow fever patients, but only by the bites of infected mosquitoes and by the artificial injection of diseased blood. The causal organism has not yet been discovered on account of its being a filterable virus. It is known, however, that a 12-day incubation period is required in Stegomyia before its bite becomes infectious to a second person. Moreover, the mosquito can obtain infected blood from a patient during only the first three days of his disease. Based on these facts, the control of yellow fever has become an easy matter. The patients are isolated as soon as the disease appears, and standing water in which Stegomyia might develop is treated with kerosene. Besides, all rooms in the building and adjacent buildings are fumigated, for the purpose of destroying living mosquitoes. Culex Mosquito and Filariasis: The tropical disease, filariasis, is caused by a minute nematode worm, Filaria, which lives in the blood of man and certain species of Culex (C. fatigans). The worms escape from the mid-intestine of the mosquito into the muscular tissue where they grow for two or three weeks. They then migrate to other portions of the body and often collect at the base of the proboscis, whence they are carried into the human blood circulation. Sometimes the worms become three or four inches long and obstruct the lymphatic canals, causing elephan- tiasis, characterized by enormous sweUings of the legs, arms and other parts of the body. body." ga. Mature microgametocyte, preparatory to forming microgametes. gb. Resting cell, bearing six flagellate microgametes (male). lo. Fertilization of a macrogamete by a motile microgamete. The macrogamete next becomes an ookin- ete. II. Ookinete, or wandering cell, which penetrates into the wall of the stomach of the mosquito. 12. Ookinete in the outer region of the wall of the stomach, i.e., next to the body cavity. 13. Young oocyst, derived from the ookinete. 14. Oocyst, containing sporoblasts, which are to develop into sporozoites. 15. Older oocyst. 16. Mature oocyst, containing sporozoites, which are liberated into the body cavity of the mosquito and carried along in the blood of the insect. 17. Transverse section of salivary gland of an Anopheles mosquito, showing sporozoites of the malaria para- site in the gland cells surrounding the central canal. 1-6 illustrate schizogony (asexual production of spores); 7-16, sporogony (sexual production of spores). {After Grassi atid Leuckarl, by permission of Dr. Carl Chun.) STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 53 House-fly and Typhoid Fever: Much attention has been directed in recent years to the dangers of the house-fly (Musca domestica) and other flies as agents in the trans- mission of disease. All Public Health Departments now take cognizance of the house-fly and issue warnings against its presence about the home. Epidemics of typhoid and cholera in many cities, as well as the out- breaks during the Spanish- American war brought out the fact that the house-fly was largely responsible for the troubles. The habits of this insect are such as to make its presence dangerous. It breeds in filth, and as an adult fly it feeds on all kinds of decaying and fecal matter as well as the sweets and liquids of the dining table. Its feet and proboscis are admirably adapted for carrying those bacterial germs that cause typhoid fever, cholera, dysentery, diarrhoea, tubercu- losis, etc. Moreover, it has been shown that typhoid bacilli swallowed by the house-fly when it feeds on and crawls over contaminated sub- stances survive the passage of the alimentary canal, so that "fly- specks" may contain many active typhoid germs. It has been shown that several other species of flies that frequent houses may also convey typhoid bacilli. The "little house-fly" (Fannia canicularis) , the Latrine-fly {Fannia scalaris), the blow-fly (Calliphora erythrocephala) , Muscina siabulans, the cluster-fly (Pol- lenia rudis), and the stable-fly (Stomoxys calcitrans) have all been found guilty and precautions should be taken to guard against their presence. The charges proven against the house-fly as an active agent in dis- seminating not only typhoid fever but also cholera, dysentery and tu- berculosis are overwhelming. This insect pest should, therefore, be banished from our midst. If we do not care for our own health we should at least protect the helpless children who are perhaps the greatest sufferers. (For further particulars the excellent works of Doctors Hewitt and Howard should be consulted.) Anthrax and Infantile Paralysis: The stable-fly {Stomoxys calcitrans), the horn-fly (Hcematobia serrata), gad-flies (Tabanus and Chrysops), and the black-fly (Simulium) have both piercing and sucking beaks and are true blood-suckers. As such they are liable to introduce virus into the human blood. Anthrax is a disease of many domesticated animals and of man; and it is believed that these blood-sucking flies are agents of transmission 54 ECONOMIC ENTOMOLOGY by inoculation forming malignant pustule; but the pulmonary and intestinal forms of the disease require other methods of infection. In the recent outbreaks of acute anterior poUomyeHtis or infantile paralysis in different parts of the United States and Canada the stable- fly was strongly suspected at first of being the transmitter of the causal organism. Later, however, in many experiments in which monkeys, rabbits and other rodents were inoculated by stable-flies caught in the wards of hospitals containing poliomyelitis patients, and flies that had fed on animals inoculated with the virus were allowed to feed upon healthy animals, no symptoms of the disease developed. Besides, the disease spread on some occasions in mid-winter when stable-flies could not be active agents. The present opinion is that insects play a subordinate role, if any, in spreading the disease and that it is trans- mitted by contact with infected persons. The causal organism has not yet been isolated, being filterable and ultra-microscopic like that of yellow fever. Tsetse-flies and Trypanosomiasis: Tsetse-flies (Glossina spp.) are not native to America, but belong to tropical and sub-tropical Africa. They are blood-sucking flies, closely related to stable-flies, and in- recent years have been shown to be causally related to severe diseases of both man and domesticated animals. Dr. Bruce made the important discovery that nagana, a very fatal disease to horses, cattle, dogs and donkeys in South Africa, was produced by a trypanosome carried to the blood by the bites of tsetse-flies. These trypanosomes are flagellate protozoa, and when they occur in the blood of certain warm-blooded animals set up a dis- ease called trypanosomiasis. They are carried from one host to another by certain invertebrates, such as mosquitoes, lice, fleas, and especially by such blood-sucking flies as the tsetse-flies. The Nagana disease is caused by Trypanosoma brucei and the tsetse- flies mostly concerned are Glossina morsitans and G. pallidipes. In the Congo Basin of Central Africa the terrible "sleeping-sickness" disease carries off tens of thousands of natives every year. Doctors Forde and Dutton isolated the specific causal organism of this disease, which was named Trypanosoma gambiense, and Bruce and Navarro traced the organism to the bite of the tsetse-fly, Glossina palpalis. Folsom states: "In the first stage of the disease, marked by the appear- ance of trypanosomes in the blood, negroes show no symptoms as a rule, STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 55 though whites are subject to fever. The symptoms may appear as early as four weeks after infection or as late as seven years. "In the second stage trypanosomes appear in the cerebro-spinal fluid and in large numbers in the glands, those of the neck, axillae and groins becoming enlarged. There is tremor of the tongue and hands, drowsiness, emaciation and mental degeneration. The drowsiness passes into periods of lethargy which become gradually stronger until the patient becomes comatose and dies. Some victims do not sleep excessively but are lethargic and profoundly indifferent to all going on around them." Late investigations go to show "that Glossina morsitans may act as a host for a human trypanosome which is probably identical with T. gambiense." Probably also " that some of the vertebrates other than man may harbor T. gamhiense and that there is a possibility of these things being transmitted to man" (Doane). With regard to the development of T. gambiense in Glossina palpalis it is known that "two days after biting an infected animal the fly becomes mcapable of mfectmg other animals and remains so for about 22 to 28 days, when it again becomes infective and may remain so for at least 96 days. During the infection period the salivary glands are found to be invaded with the type of the trypanosome that is found in the vertebrate blood" (Doane). Rat Fleas and Plague: Plague, known in three forms as bubonic, septicaemic and pneu- monic, is caused by Bacillus pestis which attacks rats, mice, cats, dogs and other animals. The disease is transmitted mainly by fleas, some- times by bed-bugs, and the wounds made by the bites allow entrance to plague bacilli. "Plague is primarily a disease of rats, an epidemic of plague in these animals having often been observed to precede as well as to accompany an epidemic among human beings." The recent outbreak of pneumonic plague in Manchuria showed an- other phase of infection. This disease is not dependent on fleas for its transmission, but it could be traced to an outbreak of plague in the tarabagans or marmots, a kind of squirrel. Dr. Cantlie says that Plague may develop or appear in the following stages: (i) as a disease in ani- mals; (2) as pestis minor conveyed by infected insects; (3) bubonic plague, sporadic cases, carried from animals to man by insects; (4) epi- demic bubonic plague carried from man to man by insects; and (5) 56 ECONOMIC ENTOMOLOGY pneumonic plague passing from man to man directly, or conveyed by insects. Dr. Kitasato is quoted as saying that the (Manchurian) pulmonary plague cannot spread through the air as the digestive tract is plague-proof, and that direct contact is necessary. Lice and Certain Diseases: Typhus fever is transmitted from man to man by the Body Louse {Pediculus vestimenti), and Beriberi probably by the Head Louse {Pediculiis capitis) . Ticks and Certain Fevers: Although ticks are not true insects yet they have been considered as coming under the field of the entomologist. In certain western states, viz., Montana, Idaho, Wyoming, Utah and Nevada, the Rocky Mountain Spotted Fever occurs and is produced by the bites of ticks {Dermacentor venustus, et al.) which carry spirochaetes. The African tick-fever is carried by another tick {Ornithodoros moubata), the African Relapsing fever possibly by a tick, the African East Coast fever of cattle by ticks (Rhipicephalus appendiculatus) and the Texan fever of cattle by a tick (Margaropus annulatus) inoculating cattle with the protozoan spirochjete Babesia bovis, a fact observed by Dr. Theobald Smith. Other Diseases: The terrible "hookworm" disease of the South is probably carried by the common house-fly. The causal organism {Anchylostoma diiodenale) a round worm may also enter the skin from infected soil. Pellagra is transmitted, according to many authorities, by the bites of species of black-fly {Simulium) or by the ingestion of mouldy corn. White grubs (Lachnosterna) are hosts for the thorn-headed worm {Echinorhynchus gigas) and food for swine which in turn becomes food for man. Leprosy, that most dreaded disease, is now believed to be trans- mitted by flies, fleas, mosquitoes and bed-bugs. Possibly also certain mites may be occasional carriers of the bacillus {B. leprcs). It will be seen from this account that the insects concerned in the transmission of disease are of two kinds: those, like the mosquito which transmit malaria and filiariasis, which are essential hosts of the disease organisms, and those which transmit the disease mechanically. Any insect which habitually attacks man or which may enter the house or STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 57 milking stable after having fed on human excreta is potentially a disease vector, so that we cannot too strongly emphasize the necessity of keeping all foods adequately screened and of preventing such insects as house-flies, blow-flies or mosquitoes from entering human dwellings. Besides carrying disease germs many insects may themselves cause disease in man. Many mites, lice and fleas cause dermatitis, scabies or ulcers in man. The larvae of many flies, notably the blue bottles, blow-flies, flesh flies and bot flies, cause intestinal, dermal, muscular, nasal or auricular myiasis in man. MacGregor in a recent paper (Bui. Ent. Res., Vol. viii, pp. 155-163) lists eighty organisms causing disease which may be transmitted by insects. Insect Behavior Toward Stimuli In recent years a large mass of facts regarding the behavior of insects toward their environment — both organic and inorganic — has been collected, and in a few cases this information has been of service in the control of injurious forms. In general, however, the application of such methods of control is still in its infancy stage, but it gives promise of valuable results in the near future. As the relations of insects to plants and to other insects have been discussed in previous sections attention will be confined here to the behavior of insects under the influence of environmental stimuli, such as light, heat, moisture, chemical contact, winds, etc. For some time it has been known that plants show tropistic move- ments with regard to light, heat, gravity, moisture, contact, etc. Moreover, some progress has been made toward an understanding of the processes. Plants, for example, bend toward the light because the cells on the side away from the light grow faster than those on the side next to the light. There is no conscious control of the movement by the plant. Animals, too, exhibit movements under the influence of tropic or taxic^ stimuh. In the case of insects, butterflies, bees, house- flies, and many moths and caterpillars are positively phototropic or phototactic and move toward the light, while maggots, bed-bugs and cockroaches move away from the light. * The term taxic is now more commonly used than Iropic when applied to the locomotor movements of animals under the action of stimuli, Iropic being usually reserved for the turning or orienting movements. 58 ECONOMIC ENTOMOLOGY Again, most moths move away from sunlight but move toward a lesser light such as electric or oil lamps. Davenport explains this difference by saying that " butterflies are attuned to a high intensity of light, moths to a low intensity." Loeb explains the circling of moths and other insects about a light. The stimulus orients the insect by its more intense action on the muscles next the light, and the insect then moves toward the light. Loeb states that caterpillars of the brown tail moth as they emerge from hibernation in spring are positively phototropic, but after they have eaten this response disappears, showing that taxic reactions are sometimes dependent on the state of the body. "Swaine finds that the destruction of piled logs by the wood-boring larvae of the sun-loving Monohammus can be prevented by forming a dense shade over the logs by means of brush. In his study of the army cutworm {Euxoa auxiliaris) in Alberta, Strickland found that the larvae are negatively phototropic and hide beneath the soil till about four or five o'clock in the afternoon when they come to the surface to feed. With the weaker light they become positively phototropic and a general migration in a westerly direction takes place. When food is scarce hunger may overcome their aversion to sunshine with the result that the larvae come above ground, but they still display a modified negative phototropism and migrate in a northwesterly direction. These facts are of practical value in controlling outbreaks of this insect (Hewitt)." Insects are very responsive to the stimulus of heat, i.e., they are thermotactic. Some insects respond to the stimulus of touch or contact, and are said to be either positively or negatively thigmotactic. Cock- roaches are in the habit of squeezing into narrow crevices, and Loeb mentions the case of a moth Pyrophila which also has the same habit. Chemical substances and foods also act as stimuH influencing the movements of insects. Maggots orient themselves with regard to their food and then move toward it, the orientation being the result of unequal chemical stimulation of the muscles of the two sides of the body. The deposition of eggs by most insects on certain plants is also the result of chemotropism. The house-fly and many piercing insects such as the biting flies and mosquitoes are repelled by phenol and other coal tar products. STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 59 Wheeler and Loeb give several examples of geotropism among insects. They observed that lady-birds and cockroaches at rest placed themselves on vertical rather than horizontal surfaces. Observations show that taxic reactions are very adaptive. Ants and aphids are positively phototaxic when they get wings; and honey bees are periodically phototaxic, thus leading to swarming. Ants, moreover, are strongly thermotaxic, thus securing for their brood the optimum temperature conditions. Relation of Insects to Temperature and Humidity Two important factors influencing the life of insects are temperature and humidity. Their general regulatory action has been known for a long time, but scientific data obtained in recent years enable us to speak more definitely regarding the behavior of insects toward the varying temperature and humidity of their environment. Pierce in his studies of the cotton boll weevil and other forms says: ''A careful study of the records of any species, charting for the time required for each activity and the temperature and then similarly for the humidity, will disclose temperature and humidity points of maximum efiiciency. With the boll weevil these points lie approxi- mately near 83°F., and 65 per cent, relative humidity." Ewing has found that a constant temperature of go^F. prevents the development of Aphis avencB, and that the optimum temperature for the production of the wingless agamic forms is about 65°F. The larvae of the common house-fly are killed at a temperature of io5°F., and the close-packing of manure is sufficient to prevent the breeding of flies. With regard to changes in humidity, insects vary somewhat widely in their reactions. For example, moist air is favorable to most aphids and hastens the development of the larva of the Hessian fly. On the other hand, dry seasons favor the development of the chinch bug and wheat midge. Gardeners and florists have long observed that red spiders and most species of thrips are more abundant, and hence more injurious, under warm dry conditions. The investigations of Bachmetjew show that humidity is an im- ortant factor modifying the effects of temperature, and that the 6o ECONOMIC ENTOMOLOGY metabolic activities of insects are related to both temperature and humidity. He says: "Apparently there is a degree of atmospheric humidity which being the most favorable to the maximum speed of insect metabolism should be designated as the optimum; that this opti- mum varies for each species, for each stage of each species, and for each stage of each individual." The codling moth is an example of a common insect whose develop- ment is greatly influenced by weather conditions. Even within the limits of a single state or province the rate of its development and the time of its stages are influenced by latitude, by early and late seasons, by cool and warm seasons, and by wet and dry seasons. The student will find in the observations of Simpson in Idaho, Pettit in Michigan, Sanderson in New Hampshire, Hammar in Pennsylvania and Michigan, Jenne in Arkansas, Caesar in Ontario, Headlee in Kansas, Siegler and Simanton in Maine, Brooks and Blakeslee in Virginia, and Forbes in Illinois much valuable data for investigations on the relation of insects to climatic factors. The Distribution of Insects On account of the large increase of international trade many economic forms of importance have been introduced into Canada and the United States from other countries, and as it is a matter of pubHc interest to know if such imported forms are likely to become injurious con- siderable attention has been given of late years to the investigation of this problem. The problem is not yet completely solved, but progress may be reported. The common natural means of dispersal are flight, wind, animals, and railways, etc. Many insects are able to fly long distances, many are carried by wind currents and many are transported on materials of commerce. A few examples of such dispersal may be cited. The brown-tail moth is a good flyer, and is thus able to spread rapidly. On the other hand, the female of the gipsy moth cannot fly, consequently the spread of this insect follows the lines of trade. It has been observed that the Hessian fly spreads most readily in the direction of the pre- vailing winds at the time of the emergence of adults, and that the larvae of the San Jose scale are carried by the winds. Again, warble and bot flies are transferred from one district to another by their hosts. Man STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 6 1 himself is responsible for the carrying of lice from district to district, often resulting in war time in serious epidemics. The Colorado potato beetle migrated eastward from its home in Colorado, preferring the cultivated potato to the wild solanums, and the asparagus beetles followed the lines of travel westward from the Atlantic. On the other hand, there are many barriers to the spread of insects: oceans, seas, mountain ranges and deserts are natural barriers and tend to prevent wide distribution. Climatic conditions, such as temperature and moisture, are also very important factors in insect distribution, often indirectly due to the absence of suitable food plants. The chinch bug and the Rocky Mountain locust, for example, do not thrive under moist conditions. As the habits of insects are very variable, some being limited, others almost cosmopolitan in their distribution; some sensitive to •emperature and moisture extremes, others more or less indifferent to these factors; some feeding only on one or two hosts, others more or less general feeders and therefore not so likely to be restricted in their range, the problem of the determination of probable insect distribution is not an easy one to solve. Moreover, the presence or absence of parasites complicates the problem. Dr. Merriam's map of the Life Zones of North America shows the distribution of birds and mammals and plants into seven zones running east and west, viz.: Arctic, Hudsonian and Canadian oi the Boreal region; the Transition, Upper Austral and Lower Austral of the Austral region; and Tropical (see Map).^ It must be understood, however, that the boundaries of these zones are not hard and fixed, for there is necessarily an overlapping to some extent. It is interesting to note that the great agricultural areas of Canada and the United States lie mainly in the Transition and Upper Austral zones. Recent studies go to show that in general insects tend to conform to the same zonal distribution, although several forms, such as the house-fly, mosquito, chinch bug and army-worm, range through several zones. ^ Merriam states the laws of temperature control as follows: I. "Animals and plants are restricted in northward distribution by the total quantity of heat during the season of growth and reproduction; and 2. "Animals and plants are restricted in southward distribution by the mean temperature of a brief period during the hottest part of the year." 62 ECONOMIC ENTOMOLOGY -^:::^^^^;5:^^«^S^^W^ ^..;# rc>e.V^ ^^S^^ ^^ I ^ I'.n,!.. .UI.AI. M IM KV /-oNK. .\l \l' "I- NciKI'll AMKKli-A Fig. 44. — Map of North America showing the life zones. (After Mo riam.) STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 63 As a rule, however, insects diffuse most readily in the zone in which they originated, and in the direction of least resistance. The Transi- tion and Austral zones are differentiated into an eastern humid, a western arid and a Pacific humid division and certain insects occur in one division and not in the others. As examples of the economic importance of a study of the factors of distribution of insects the cases of the imported elm-leaf beetle and San Jose scale may be given. Fernald says: "The Elm-leaf Beetle . . . thrives in the Upper Austral Zone, but is noticeably absent in the highlands of the Pennsylvania mountain regions, though it is present again west of them. To the north it has caused serious loss to the elms of New England, resulting in the appropriation of large sums for spraying of the trees to protect them from its ravages. Careful studies of this pest in Massachusetts show that while a serious menace to the life of the elms in the southern part of the state and in the river valleys, it becomes of little importance in the higher and northern parts, and many towns which formerly appropriated money for the protection of their elms from this insect have now learned that this was unnecessary, as the trees would suffer but Uttle at most, in any case. "With the San Jose Scale similar facts are now coming to light. This pest finds the best conditions for its hfe in the Lower and Upper Austral Zones, where it has caused the loss of many millions of dollars. Even in the Upper Austral territory of Massachusetts, it is one of the most destructive enemies of the fruit-grower. As we pass into the Transition Zone, however, its ravages become less severe, and by the time the centre of this zone has been reached it is of only medium importance. In this case it has seemed to those studying this problem that this insect was originally limited by the Upper Austral, but has gradually acquired some degree of resistance to lower temperatures and has thus been able to extend into the Transition Zone." As Webster has shown, the migration and diffusion of insects have occurred along four main lines. The first was from the east by way of New York or one of the North Atlantic states and the open pathway into the interior past lakes Ontario and Erie. Examples of such migration are the imported cabbage butterfly, the two species of asparagus beetles, the clover-leaf weevil, the clover-root borer, the Hessian fly, the horn fly and the willow curculio. The second line was northward from the West Indies by way of Florida up the Atlantic coast, bringing in many beetles, scale insects, the harlequin cabbage bug and other Hemiptera. The third Hne was northward from Central 64 ECONOMIC ENTOMOLOGY and South America by way of Mexico, passing up the Mississippi valley or up the western valleys. Examples of such migration are the Diabroticas, the cotton boll weevil, the Argentine ant, the potato beetle, Halisidota, harlequin cabbage bug and the chinch bug. The fourth was southward from Asia by way of Alaska. Examples of such a diffusion are certain lady-birds, Lina spp. and Silpha spp. Regarding the fauna of British Columbia E. M. Walker believes it represents a mingling of Asiatic, Californian and Mexican types. With regard to insects that have come in from foreign countries it is generally true that they confine themselves to zones similar to those from which they have come. Of these mention may be made of Crio- ceris asparagi, Pieris rapce, Hylastinus obscurus, the warble" and bot flies, the San Jose scale, and the gypsy and brown-tail moths. Some forms, such as the codling moth and other insects, tend to become cos- mopolitan, but they seldom become epidemic outside of their special zones. Similarity of climatic conditions in corresponding zones of two continents renders it easy for species introduced from one to the other to gain a footing, as the absence of native parasites affords an oppor- tunity for excessive multiplication. The influence of elevation on the distribution of insects is seen in the southward extension of the zones in hilly or mountainous regions. In an understanding of the distribution of many northern forms often isolated on summits south of their normal zone geological history comes to our aid. The great Tertiary extension of land areas in the north- east and the northwest, making land connections with Europe and Asia, permitted northern forms from these continents to pass to America, and the advance of the Great Glacier southward during the Glacial Period forced many northern forms southward, some of whom were left stranded on mountain summits on the retreat of the ice. Methods of Studying Economic Insects It has been already pointed out that one of the characteristics of modern-day investigations in economic entomology is the introduction of the "field station" method, whereby each pest is studied under natural conditions both in the open field and in the laboratory. By this method it is possible to study all or most of the factors that play a part in the life of both host and pest. No phase is too trivial for STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 65 examination, for it may sometimes happen that apparently trivial and minor factors turn out to be important; for example, the discovery of a preoviposition period for many Diptera furnishes a means of con- trolling them at this vulnerable period. An important part of the equipment of the economic entomologist is a knowledge of the principles of "ecology" which enables him to analyze and scrutinize the various factors that play upon insects. The ecological sciences that have a more or less direct bearing upon economic entomology are Botany, Zoology, Chemistry, Physics, Geology and Geography, and their outgrowths, Bacteriology, Forestry, Meteorology, Physiology, and the group termed Agriculture. While a knowledge of these sciences is valuable in the study of in- sect problems it must necessarily be general in its character and in- sufficient for the solution of many of the more difficult problems. The worker should, therefore, confer with speciaHsts in other depart- ments. Especially is this necessary in deahng with measures of con- trol. Sometimes recommendations are made which are at variance with the most approved farm practice. By consultation with an agronomist, horticulturist or forester such conflicting recommenda- tion would not be given to the pubHc but would first be revised to meet all requirements. In the study of insects of farm crops, for example, the investigator, working along his own line, frequently reaches a position where he cannot make further progress without more information from workers in other branches and from experienced farmers. Such information may relate to methods and action of fertilizers, methods of cultivation and rotation, meteorological and physiographic influences, and the practical application of measures of procedure. Similarly in dealing with orchard insects progress in investigation can only be made when there is full co-operation with the expert horticulturist, the orchardist, the pathologist and others, who are able to give valuable advice and assistance. As one might expect, every kind of insect demands its own par- ticular method of investigation, for no two kinds of insects are oper- ated upon by the same factors. Hence the successful investigator must be able to contrive simple but effective devices for the determination of the various factors. Costly insectaries and appliances are not abso- lutely necessary; on the other hand, the tendency among the best work- 66 ECONOMIC ENTOMOLOGY ers is to use inexpensive appliances. The most important consideration in the rearing of insects for the purpose of ascertaining their Hfe history is to make conditions as nearly natural as possible. Cages of various kinds covered with muslin or wire netting are in common use. Some may be flower pots and lamp chimneys in which the host plants are Fig. 45. — Types of underground breeding cages, i, 15-inch pots with wire ^^screen cover tops; 2, 15-inch pots with cyhnder-shaped tops. (After Davis.) growing; others, breeding cages of larger size and more elaborate construction. In the study of underground forms such as white grubs and wire- worms the cages are usually buried to the full depth in the earth, Davis has found large flower pot cages, deep cylinder-shaped cages and STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 67 Fig. 46. — Insect breeding cage, a, Sliding glass door; b, galvanized iron base; c, galvanized iron holder for records; d, wooden base; e, wooden bottom detachable. Sides are covered with cheesecloth. {After Webster.) Fig. 47. — A gasoline or electric trap lantern with attachment of four cups for nsects, which fit into each other and are separated by netting of different sizes, and one for cyanide at the bottom. {After photo by Davis.) 68 ECONOMIC ENTOMOLOGY cages constructed of wire gauze useful. One-ounce tin salve boxes are employed to study the habits of the grubs, their growth and moults. In the breeding of aphids and other insects which readily succumb to heat, the cages are placed in "shelters" covered with a canvas screen so as to permit free air circulation (Figs. 45-49)- When trees are convenient the shelters may be placed under them and the screens removed. The rearing and distribution of parasites of insects demands special contrivances which may be easily made. Much valuable information Fig. 48. — Insectary and aphid breeding shelter, shuwiug canvas curtain rolled up. {Photo by J. J. Davis.) is available as a result of the experiences of the workers in the Parasite Laboratory at Melrose Highlands, Mass. The economic entomologist should be a good photographer, and the laboratory should possess a full photographic outfit and a dark room. Camera records are among the most valuable. A very important part of the work of the investigator is the keeping and filing of records of the collections, experiments and observations. Two catalogues of the collections — the Accessions Catalogue and STRUCTURE, GROWTH AND ECONOMICS OF INSECTS 69 the Species Catalogue — and an Experiment Record of the experiments that are conducted should be kept. The Loose-leaf filing system is one that is admirably adapted for these purposes. The observational notes are best made on separate detachable slips of a note book that can be conveniently carried in the pocket. These slips are torn off and filed in card index trays under the name of the insect discussed. This method saves unnecessary transcribing, is Fig, 49. — A large breeding cage used in the study of locusts, army worms, etc. {Photo by J, J. Davis.) simple, and serviceable in matters of correspondence and the prep- aration of reports and bulletins. Three types of collections should be made: (i) the reference collec- tion in standard cases such as the Schmitt, the Comstock or other form of box in which the specimens are arranged in systematic order accord- ing to the latest check lists; (2) the economic collection where the speci- mens are arranged according to host, where the life-stages and the work of the insect are given prominence; and (3) the illustrative collection in Riker mounts for lecture purposes. PART II TABLES FOR THE IDENTIFICATION OF INSECTS INJURIOUS TO FARM, GARDEN AND ORCHARD CROPS, ETC. I. INSECTS INJURIOUS TO CEREAL CROPS {Wheat, Rye, Barley, and Oats) (Consult Bull. 52 C. E. F. Ottawa, Bull. 44 W. Va.. and Farmers' Bull. 132 U. S. Dep. Ag.) Roots: (a) Plants stunted, yellow, and withered or dead; roots eaten. 1. Smooth, slender, wire-like, six-legged worms present in the soil. — Wire- worms, p. 293. 2. Presence in the soil of large soft-bodied whitish grubs with brown heads, and hinder portion of body thicker than fore end. When disturbed grubs curl up. — White Grubs, p. 302. 3. Large dirty-brown maggots, ^-i inch long. — Meadow Maggots, p. 242. Stems and Leaves: (a) Young plants dwarfed, and color changed to yellow or brown; stems shrivelled at the base, often bent or broken off; flaxseed objects found embedded at or near the base. Oats immune. — Hessian Fly (Mayetiola destructor), p. 245. (b) Stems above last joint dead, and the heads white — "silver top" or "white head" disease. Greenish maggot in stem above last joint. — Wheal Stem Maggot {Meromyza americana) and American Frit-fly {Oscinis carbonaria), pp. 260-1. (c) Swellings or galls on the joints, and stems bent or broken before harvest. — Joint Worm {Isosoma tritici), p. 354. {d) Stems broken down and tunnelled, blackish near the joints; heads turning white; presence in tunnel of yellowish-white larva of saw-fly; oats immune. — Western Wheat-stem Saw-fly (Cephus occidentalis), p. 349. (e) Leaves sickly and whitish; the presence of small red and larger black- and-white bugs. — Chinch Bug (Blissus leticopterus), p. 161. (/) Stems and leaves sickly; the presence of many green or yellowish-green plant-lice. — Wheat Plant-louse {Aphis avence), English Grain Plant-louse (Macrosiphum granarium) , p. 142. (g) Stems and leaves eaten by large dingy striped caterpillars. — Army-worm {Cirphis unipuncta), p. 190. {h) Leaves eaten by locusts or grasshoppers. Red-legged and other Grass- hoppers. — {Melanoplus femur-rubrum et al.), pp. 109-113. 71 72 ECONOMIC ENTOMOLOGY Heads: (a) Heads turn white and grains are shrivelled or imperfectly filled. — Wheat Stem Maggot {Meromyza americana) and American Frit-fly {Oscinis car- bonaria), p. 261. (b) Heads shrivelled and blighted, and imperfectly filled; the presence of orange-colored maggots. — Wheat Midge (Diplosis iritici), p. 249. (c) Heads covered with green plant-lice. — Grain Louse {Aphis avetice), p. 142. (d) Heads turn white; minute dots or lines on leaves usually run parallel with the veins and remain white; the work of minute insects. — Grass Thrips (Anaphothrips striatiis), p. 119. (e) Spotting of the leaves, spots whitish at first, turning brown or black. — Six-spotted Leaf-hopper {Cicadula 6-notata), p. 154. (/■) Heads blasted and stems withered; the presence of frothy masses on the stems. — Grass-feeding Froghop per {Philcenus lineatus), p. 153. II. INSECTS INJURIOUS TO INDIAN CORN OR MAIZE (Consult Bull. 44 Illinois Agric. Exper. Station) Planted Seed: (a) Plant fails to come up after planting; grain destroyed by a maggot which eats out the interior. — Seed-corn Maggot {Phorbia fusciceps), p. 277. {b) Plant fails to come up, or the young plant suddenly wilts after it is above ground; the presence of hard, smooth, yellowish, wire-like worms. — Wire-worms spp., p. 293. Roots: (a) Young plants killed or withered; roots eaten. — White Grubs or Wire-worms, P- 303- (b) Young plants unequal in growth; roots dwarfed without external injury; presence of ants. — Corn-root Louse {Aphis maidi-radicis) . Stalks: {a) Plants cut off near surface of ground. — Cutworms, p. 185. {b) Plants unthrifty and covered with greenish plant-lice. — Corn Plant-louse {Aphis maidis), p. 142. (c) Stalks punctured and slit. — Corn Bill Bugs {Sphenophorus spp.), p. 338. {d) Pith of stalk and pedicel of cob tunneled by a flesh-colored caterpillar, terminal internode broken. — European Corn Borer {Pyrausta nubilalis). Leaves: {a) Leaves thickly covered with green plant-lice. — Corn Plant-louse {Aphis maidis). {b) Leaves eaten. — Army-worm {Cirphis unipuncta) and Grasshopper, p. 190. (c) Leaves perforated by round or oblong holes arranged in parallel trans- verse rows. — Corn Bill Bugs, p. 338. {d) Leaves wilted and brownish, sometimes sickly and whitish; the presence of small red and larger black-and-white bugs. — Chinch Bug {Blissus leuco- pterus), p. 161. (e) Leaves wilted and brownish caused by the maggot of a syrphid fly. — Corn-feeding Syrphid Fly {Mesogramma politus), p. 251. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 73 Ears: (a) Developing kernels eaten; presence of much excrement. — Corn Ear Worm (Heliothis ohsoleta), p. 195. (i) Stalks of ears covered with plant-lice. — Corn Plant-louse {Aphis maidis), p. 142. (c) Developing kernels eaten; cob and tassel stalk tunneled. — European Corn Borer {Pyrausta niihilalis), p. 212. III. INSECTS INJURIOUS TO CLOVER AND ALFALFA (Consult Bull. 134 Illinois Agric. Exper. Station, 1909) Roots: (a) Second year plants wilted and dead, breaking off easily at the crown. Main root tunnelled and occupied by white footless grubs or little dark brown cylindrical beetles. — Clover Root Borer (Hylastinus ohscurus), p. 341. {b) Plants wilted and leaves dead, mealy bugs near crown of root. — Clover Root Mealy Bugs (Pseudococcus trifolii), p. 133. Stems: (a) A long burrow with brown discolored walls in the pith of the stem which falls to the ground prematurely. — Clover Stem Borer (Languria mozardi). (b) Stems cut off or eaten. — Cutworms, Army-worms {Cirphis tinipuncta) and Grasshoppers, p. 109. (c) Stems and leaves withered and dead; plants covered with large green long-legged plant -lice. — Pea or Clover Plant-louse (Macrosiphum pisi), p. 149. Leaves: (a) Leaves fuU of round holes, and edges gnawed. — Clover Leaf Weevil (Phy- tonomus punctatus), p. 331. (b) Leaves eaten and with a ragged appearance. — Grasshoppers, p. 109. (c) Leaves folded along midrib, yellowish or brownish, with white or orange maggots or silken cocoons within the folds. — Clover Leaf Midge (Dasyneura trifolii), p. 248. Heads and Seed: (a) Florets at blossoming-time green and undeveloped; the ovaries empty or with an orange pink or whitish maggot. — Clover Seed Midge (Dasyneura leguminicola), p. 246. {b) Florets withered and seeds undeveloped; the presence of frothy masses on stems. — Meadow Fro ghop per {Philanus spumarius), p. 153. (c) Seeds eaten, becoming brown, brittle, and hollow; affected seeds dull brown and often misshapen and of small size; maggot minute, white and footless. — Clover Seed Chalcid (Bruchophagus funebris), p. 355. {d) Unopened blossoms destroyed, a cavity eaten in the head. — Clover Seed Caterpillar (Laspeyresia inter stitictana), p. 228. Stacked or Stored Clover Hay: (a) Hay containing white silky webs and particles of excrement. — Clover Hay- worm (Hypsopygia costalis), p. 208. 74 ECONOMIC ENTOMOLOGY IV. INSECTS INJURIOUS TO PEAS AND BEANS Planted Seeds: (a) Plant fails to come up, due to work of White Grubs or Wireworms, or Bean or Seed Corn Maggot, p. 277. Stalks and Leaves: (a) Plants cut off at night near surface of the ground. — Cutworms, p. 185. (b) Plants unhealthy, often killed by sucking lice. — Pea Louse {Macrosiphum pisi), p. 149. (c) Plants (beans) sickly and sooty, caused by a black aphis feeding at the tips at blossoming time. — Bean Aphis {Aphis rumicis), p. 148. Seeds: (a) Seeds (peas) within the pod partly eaten and web-covered; pellets of excre- ment about injured seed. — Pea Moth {Las peyresia nigricana), p. 226. {b) Seeds within the pod (peas) perforated with holes; footless grubs within. — Pea Weevil {Bruchus pisorum), p. 319. (c) Seeds (Beans) perforated with (sometimes many) holes; footless grubs within. — Bean Weevil {Bruchus obtectus), p. 319. V. INSECTS INJURIOUS TO STORED GRAIN PRODUCTS (After Girault, Bull. 156 Illinois Ag. Exp. St.) Moths or Millers, {a) Caterpillar small, whitish, living in grains of corn or wheat, pupating within the grain, and emerging through a round hole covered with silk at or near the tip of the kernel. Adult moths grayish clay- yellow, small. — Angoumois Grain Moth {Sitotroga cerealella), p. 214. {b) Caterpillars, spinning much silk, usually forming a silken tube to which they retire; this tube covered with food particles. Living in flour, meal, chaff, sometimes among grain, or in food substances. Full-grown caterpillars make a cocoon. 1. Caterpillar free-living usually not concealed within a silken tube, olive-green to pinkish, infesting grain or meal, webbing particles together, covering bags of grain with a web of silk and generally scattering silk in all directions. The moth is brown and gray. Cocoon elliptical, slender, fragile and of clear silk. — Indian Meal Moth {Plodia inter ptmctella) , p. 214. 2. Caterpillars living in densely woven silken cases covered with particles of the food substance. Common in flour or chaff in corners. (i) A yellowish white to pinkish caterpillar in flour, webbing it together and forming a cocoon covered with particles of flour. Moth dark grayish. — Mediterranean Flour Moth {Ephestia kuehniella), p. 213. (2) A soiled grayish caterpillar, darker at each end, living in chaff or other vegetable debris in dark damp places, IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 75 securely webbing the food substance together, so that it becomes matted; larval case and cocoon completely hidden, covered with the food substance. Adults very beautiful and delicately colored moths. — Meal Snout Moth {Pyralis farinalis), p. 208. Beetles or Weevils. (a) Small insects living in kernels of grain, or among grain and other stored products. 1. A very small, fat, humped-backed grub, in kernels of wheat or corn; yellowish- white, legless, and wrinkled, unable to crawl; pupa within the kernel. Adult smaller than a grain of wheat, with a snout, and elbowed feelers attached to the snout. (i) Adult beetle chestnut-brown, without spots on its upper wings. Slightly larger than the next, more common in the North. — Granary or Black Weevil (Calandra granaria), p. 337- (2) Adult beetle somewhat duller brown than the preceding with four reddish spots, one on each outer corner of the upper wing. A southern species. — Rice or Spotted Weevil (Calandra oryza). 2. Small, more or less slender, somewhat flattened grubs, with dis- tinct head and thoracic legs, crawling about in the debris of var- ious grains or their products, or in vegetable foodstuffs. Adults flattened, longer than wide, the head not prolonged into a snout. They occur with the grubs, actively feeding. (i) Grub uniform in color, whitish, about one-fourth inch long, slender, its head narrower than the first body segment; pupa with the thorax not toothed laterally, but with most of the abdominal segments bearing a tooth-like lobe, acute at each outer corner and toothed along its sides. Adult beetle active, smooth, elliptical, and reddish brown. — Confused Flour Beetle (Tribolium confusum), p. 328. (2) Grub whitish, with a rectangular yellowish area on each segment above, only the margin whitish as seen from above; head broader than first body segment. Pupa bears along each side of the thorax and abdomen a series of stout lobe-like teeth, which are cylindrical- rectangular and blunt. Adult beetle smaller than in the preceding species, color dark chocolate-brown, sides of the thorax saw-toothed.— 5flw-/oo//rc(/ Grain Beetle (Silvanus surinamensis), p. 326. (3) Grub dull white with a dark brown head; fleshy, three- fourths inch long; posterior end with two dark horny points. Pupa white, adult beetle, elongate, depressed. 76 ECONOMIC ENTOMOLOGY nearly black, one-third inch long. — Cadelle (Tenebroides mauritanicus) , p. 326. (b) Large insects, concealed in the bottoms of bins, corners, and the like, feeding upon flour, meal or bran. Adults large black beetles; the lar- vas, large, cylindrical, wormlike creatures, resembling wireworms. 1. Adult not quite black in color, shining, its third antennal joint not quite twice as long as the second; larva light yellowish, shining. — Yellow Meal-worm Beetle {Tenebrio molitor ), p. 327. 2. Adult black and without luster, its third antennal joint thrice as long as the second; larva very dark, shining. — Dark Meal-worm Beetle {Tenebrio obsctiriis), p 328. VI. INSECTS INJURIOUS TO ROOT CROPS (Turnips, rape, mangels, and carrots) (Consult Bull. 52 C E. P., Ottawa, and Bull. 60, 111. Exp. Sta.) Roots: (a) Tips of roots of young carrots with rusty patches on surface, or rust colored tunnels in the pulp, due to slender yellowish- white maggots. — Carrot Rust Fly {Psila rosce), p. 262. (6) Roots of turnips bored or tunnelled by minute grubs or maggots. — Turnip Flea Beetle (Phyllotreta vittata); Cabbage Root Maggot {Phorbia brassicce), P- 273- (c) Roots cut off. — Wireworms, White Grubs, Cutworms, pp. 185, 293, 302. Stem and Leaves: (a) Young plants cut off at the ground. — Cutworms, p. 185. (b) Surface of first leaves of turnip and rape eaten into small holes by small active black striped beetles. — Turnip Flea Beetle {Phyllotreta vittata), p. 314. (c) Leaves partly consumed by pale-green caterpillars. — Cabbage Worm {Pieris rapce), p. 175. {d) Leaves eaten by caterpillars with black and yellow stripes. — Zebra Cater- pillar {Ceramica picta), p. 188. (e) Leaves wilt and turn yellow, with presence of greenish lice.- — Turnip Plant- louse {Aphis brassica), p. 148. (/) Young leaves eaten into holes and irregular blotches by small active green caterpillars. — Diamond Back Moth {Plutella mactilipennis), p. 232. (g) Under-surface of leaves covered with a very fine loose web; leaves yellow- ish in patches, and minute red objects present. — Red Spiders, p. 367. (A) Leaves eaten by red beetles with black stripes (Prairie Provinces). — Red Turnip Beetle {Entomoscelis adonidis), p. 309. VII. INSECTS INJURIOUS TO THE POTATO CROP Tubers: {a) Surface of tuber eaten and eyes sometimes destroyed so that growth does not take place; or holes bored in the tuber. — White Grubs, Wireworms, Millipedes, p. 369. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 77 Stalks and Leaves: (a) Stalks cut off at the ground. — CiUworms, p. 185. {b) Leaves eaten and infested with reddish soft grubs and striped beetles. — Colorado Potato Beetle (Lepiinotarsa decemlineata) , p. 308. (c) Leaves riddled with small holes or surface eaten in spots by small active jumping black beetles. — Potato Flea Beetle (Epitrix cucumeris), p. 313. {d) Leaves eaten and with a ragged appearance; presence of long black or striped soft beetles. — Blister Beetles {Epicauta spp.), p. 325. (e) Stalk wilts and dies, tunnel in stalk near the ground, and presence of a white footless grub. — Potato Stalk Borer {Tricliobaris trinotata), p. 334. if) Green plant-lice on the leaves; migrating to the rose. — Potato Plant-louse {Macrosiphum solanifolice) . VIII. INSECTS INJURIOUS TO GARDEN VEGETABLES [Under the term "Garden Vegetables" may be included Asparagus, Beets, Cabbage, Cauliflower, Celery, Cucumber, Onion, Parsnip. (Carrots, beans, peas and potatoes have already been considered.)] Roots: (a) Roots of cabbage and cauliflower and bulb or base of onion mined by white maggots. — Root Maggots (Phorbia brassicce and Phorbia cepetorum), p. 273. {b) Roots of cucumber, squash, melon and pumpkin eaten, and plants fail to come up. — White Grubs, Wireworms. [c) Roots of cucumber, etc., gnawed and mined, plants wilt and die. — Striped Cucumber Beetle {Diabrotica vittata), p. 307. Stems and Leaves: (a) Young plants cut off near surface of ground. — Cutivorms. (b) Stalks, vines and leaves of cucumber, etc., eaten, and base, mined by small white grubs. — Cucumber Beetles (Diabrotica spp.), p. 307. (c) Vines of cucumber, etc., wilted, and presence of large dark stink-bugs on leaves. — Squash Bug (Anasa tristis), p. 160. (d) Leaves and vines of cucumber, etc., sickly and dirty, under surfaces infested with greenish-black lice. — Melon Plant-louse {Aphis gossypii). (e) Surface of leaves of cucumber, etc., eaten by small black beetles. — Cucumber Flea Beetle (Epitrix cucumeris), p. 313. (/) Leaves of cabbage, etc., ragged, eaten by pale-green caterpillars. — Cabbage Worm (Pieris rapa), p. 175. (g) Leaves of cabbage, etc., wilted, and under-surface covered with greenish plant-lice. — Cabbage Plant-louse (Aphis brassicce), p. 148. IX. INSECTS INJURIOUS TO THE APPLE (Consult Manual of Fruit Insects by Slingerland and Crosby) Roots: (a^l Bluish-white mouldy lice causing knots or swellings on the smaller roots. — Woolly Aphis (Schizoneura lanigera), p. 145. 78 ECONOMIC ENTOMOLOGY (b) Large white grubs feeding on the roots of nursery stock. — White Grubs {Lachnoslerna spp.), p. 302. Trunk, Branches and Tmigs: (a) A green curiously shaped bug producing longitudinal slits in the bark; eggs laid under the edges of the slits. — Buffalo Tree Hopper {Ceresa hubalus), P- 157- {b) White woolly patches on the twigs which are usually scarred. — Woolly Aphis {Schizoneura lanigera), p. 145. (f) Green soft-bodied sucking insects in clusters on young growths, particularly at ends of twigs, producing distortions. — Apple Aphids (Aphis mali, A. sorbi and A. avencs), p. 143. {d) Snout beetles gnawing off the bark in patches. — Imbricated Snout Beetle {Epicarus imbricatus). (e) Fixed to bark: 1. Scales round and gray and black producing an ashy gray incrusta- I tion on the bark. — San Jose Scale (Aspidiotus perniciosus) , p. 126. 2. Bark rough with mussel-shaped scales. — Oystef-shell Scale (Lepido- saphes ulmi), p. 124. 3. Bark scurfy with white scales. — Scurfy Scale (Chionaspis furfura), p. 125. (/) Making tunnels in the wood: 1. Large square-headed legless borer at or near the ground in tunnels, with sawdust-like excrement. — Round-headed Borer (Saperda Candida), p. 320. 2. Large flat-headed legless borer in upper trunk in tunnels with saw- dust-like excrement. — Flat-headed Borer (Chrysobothris femorata), p. 300. 3. Large grub in decaying wood. — Eyed Elater (Alaus ocidatus) and Rough Osmoderma (Osmoderma scabra), p. 305. 4. Making tunnels between the bark and wood. Fruit Bark Beetle {Eccoptogaster rugulosus), p. 339. Buds: (a) Light green caterpillars with brown head and shield, folding together the opening leaves and feeding within. — Oblique Banded Leaf-roller (Cacoecia rosaceana), Fruit-tree Leaf Roller (C. argyrospila), and Leaf Grumpier {Mineola indigenella) , p. 230. (b) Brownish caterpillar with black head and shield eating the centre of the bud, or tunnelling it. — Eye-spotted Bud Moth {Tmetocera ocellana), p. 225. (c) Measuring worms, eating leaves of buds. — Canker Worms (Alsophila pome- taria and Paleacrita vernata), p. 205. {d) Caterpillars feeding within pistol-shaped cases and eating irregular holes in the bud leaves. — Pistol Case Bearer {Haploplilia malivorella), p. 235. (ej Caterpillars feeding within cigar-shaped cases and eating small round holes in the bud leaves. — Cigar Case Bearer (Haploptilia fletcherella), p. 234. (/") Click beetles feeding on buds. — Corymbites spp., p. 297. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 79 Leaves: (a) Gregarious caterpillars: Caterpillars protected by webs: 1. Webs in forks of branches in spring. — Tent-caterpillar {Malacosoma americana) , p. 203. 2. Webs covering the leaves in summer and early autumn. — Fall Weh Worm (Hyphantria textor), p. 181. 3. Leaves partly eaten and drawn together by a web. — Palmer Worm {Dichomeris pometella), p. 215. Caterpillars not protected by a web: 1 . Clustered on limbs. — Yellow-necked Cater pillar{Datana ministra) , p . 1 98. 2. Red-humped Apple-tree Caterpillar {Schizura concinna), p. 199. 3. Forest Caterpillar {M. disstria), p. 204. (6) Solitary caterpillars: Protected caterpillars: 1. Mining within the leaf, pupa inside of folded leaf. — Apple Leaf Miner {Tischeria malifoliella), p. 235. 2. Mining within the leaf, mature larva and pupa within a small oval seed-like body. — Resplendent Shield Bearer (Aspidisca splendoriferella), p. 232. 3. Feeding within a pistol-shaped case which stands out from the leaf. — Pistol Case Bearer {Haploptilia malivorella) , p. 235. 4. Feeding within a cigar-shaped case which stands out from the leaf. — Cigar Case Bearer {Haploptilia jletcherella), p. 234. 5. Feeding within a folded leaf. — Leaf Roller {Teras malivorana), Caccecia spp., Apple Leaf Sewer (Ancylis nubeculana), p. 230. 6. Feeding within a tube of silk, open at both ends, on epidermis and inner tissues, leaving the veinlets. — Bud Moth {Tmetocera ocellana), p. 225. 7. Feeding on tissues of leaves beneath a silk web. — Apple Leaf-skele- tonizer (Psorosina hammondi), p. 213. 8. Brown caterpillar feeding within a crooked black case and attached to twigs in winter. — Leaf Crumpler (Mineola indigenella) , p. 213. Unprotected caterpillars: 1. Measuring worms in spring, feeding in the daytime. — Canker Worms {A. pometaria and P. vernata), p. 205. 2. Sleek i6-legged caterpillars, feeding at night. — Cutworms, p. 186. 3. Large green caterpillar, covered with spiny tubercles. — Cecropia Moth {Samia cecropia), p. 180. 4. Large apple-green caterpillar with white oblique stripes on sides. — Polyphemus Moth {Telea polyphemus), p. 180. 5. Hairy caterpillar with long black tufts over head and tail. — Tussock Moth (Hemerocampa leucosligma) , p. 202. 6. Large green caterpillar with a reddish-brown horn at tail, and seven oblique stripes on each side. — Apple Sphinx {Sphinx gordius), p. 178. 8o ECONOMIC ENTOMOLOGY 7. Small caterpillars with brown head and yellowish-green body, feeding on leaves. — Apple-leaf Bucculatrix {Bucculatrix pomifoliella), p. 236. (c) Plant-lice. Greenish or rosy colored sucking insects feeding on the under sides of leaves, often distorting them. — Aphis mali, A. sorbi, and A. avencB, P- 143- (i"! Beetles: 1. Large brown beetles feeding at night on leaves. — May Beetles {Lach- nosterna spp.), p. 302. 2. Small brown beetles, feeding at night. — Leaf Beetles, p. 301. (e) Miles. Oval reddish-brown mites feeding on leaves causing them to become blanched, yellow or sickly. — Clover Mite {Bryohia pratensis), p. 367. Fruit: (o) Boring tunnels through thefrtnt: 1. Tunnels made mostly about the core; made by a pinkish caterpillar three-fourths inch long when full grown; brown excrement often visible at opening at blossom end of apple. — Codling Moth {Carpocapsa ponionella), p. 219. 2. Tunnels not so deep as in i, often blotched mines near the surface. Made by caterpillars not so large as codling worms. — Lesser Apple Worm {Laspeyresia prunivora), p. 227. 3. Tunnels irregular and numerous made by a maggot. — Apple Maggot {Trypeta pomonella), p. 266. (b) Puncturing the fruit: 1. Four-humped beetles puncturing the fruit and distorting it. — Apple Curculio (Anthonomus quadrigibbus), Plum Curculio {Conotrachelus nenuphar), p. 329. 2. Purplish spots about the circular scales. — San Josi Scale {Aspidiotus perniciosus), p. 126. 3. Puncturing and deforming the fruit.- — Several species of Capsida (False tarnished plant bug and the apple red bugs) ; and Syntomaspis druparum (p. 165). (c) Eating holes in the fruit: 1. Large light yellow or apple-green caterpillars with a narrow cream colored stripe along middle of the back. — Green Fruit Worms {Grap- tolitha spp.j, p. 197. 2. Yellowish hairy beetle one-half inch long. — Bumble Flower Beetle {Euphoria inda), p. 305. 3. Green worm-like saw-fly larva hibernating in cavities scooped out of apple. — Dock False Worm {Ametastegia glabrata), p. 347. X. INSECTS INJURIOUS TO THE PLUM Roots: (a) Burrows made by a caterpillar about the crown of the roots, occasionally in young trees. — Peach-tree Borer (Synanthedon exitiosa), p. 216. Trunk, Branches and Twigs: (a) Tunnels in the wood by flat-headed grubs; sawdust-like excrement at the mouth of tunnels. — Flat-headed Borer {Chrysobothris femorata), p. 300. IDENTIFICATION OP INSECTS INJURIOUS TO CROPS 8 1 (b) Tunnels in the bark by small legless grubs.— Fr«/; Bark-bcelle {Eccoplo- gaster rugulosus), p. 339. (c) Bases of buds perforated, bark becomes discolored, and leaves and fruit wither. — Pear Blight Beetle {Anisandrus pyri), p. 340. (d) Fixed to bark: 1. Flat or saddle-shaped, or hemispherical dark-brown scales; wintering forins small and flattish. Large scales appear after mid-summer, brittle, contain only a whitish dust or empty egg-shells. — Fruit Lecanium {Lecanium corni), p. 129. 2. Ashy-gray appearance of bark of badly infested trees due to small gray or black circular scales. — San Jose Scale {Aspidiotus perniciosus) , p. 126. 3. Mussel-shaped scales, with whitish eggs underneath in winter. — Oyster Shell Scale (Lepidosaphes ulmi), p. 124. 4. Bark scurfy with scales with purplish eggs underneath in winter. — Scurfy Scale {Chionaspis furfiira), p. 125. (e) A grass green curiously shaped bug producing longitudinal slits and eventu - ally oval-shaped scars on the back of the twigs. — Buffalo Tree-hopper {Ceresa bubalus), p. 157. Leaves: (a) Feeding in Colonies. 1. Caterpillars protected by webs in the forks of branches. — American Tent-caterpillar (Malacosoma americana), p. 203. 2. Caterpillars protected by webs covering the leaves. — Fall Web-worm {Hyphantria textor), p. 181. 3. Not protected by webs; greenish lice with sucking mouths. — Plum- leaf Aphis {Aphis prunifolii). {b) Solitary. 1. Measuring worms, feeding in the day time in spring. — Canker Worms (Alsophila pomelaria), p. 205. 2. Fat greasy caterpillars, feeding at night in spring. — Cutworms, p. 192. 3. Hairy caterpillars with long black plumes over head and tail. — Tussock Moth {Hemerocanipa leucostigma), p. 202. 4. Large buzzing beetles. — June Beetles {Lachnosterna spp.), p. 302. 5. Large apple-green caterpillar, with a horn near the tail, and with seven broad oblique white stripes along each side. — Plum-tree Sphinx (Sphinx drupiferarum), p. 178. Other larvae are occasionally found feeding on the leaves of plum. — The Viceroy (Limenitis disippus), Polyphemus and Cecropia, p. 180. Fruit: (a) A snout-beetle puncturing and making a crescent-shaped slit in the skin of the young fruit which soon drops. — Plum Curculio {Conotrachelus nenuphar), P- 329- (6) Making a round hole in the young fruit. — Plum Gouger [Coccotorus scutel- laris). 82 ECONOMIC ENTOMOLOGY (c) A medium sized beetle eating holes in the ripe fruit.- — Bumble Floiver-hcdle {Euphoria itida), p. 305. {d) A long-legged straw-colored beetle eating holes in the half-ripe fruit. — Rose Chafer {M acrodactylus snhspinosus), p. 305. XI. INSECTS INJURIOUS TO THE CHERRY Rool: (a) A thick whitish grub, with brown head and legs, feeding in decaying roots. Beetle large with powerful mandibles. — Stag Beetle (Lucanus dama), p. 318. {b) A large white fleshy grub, with reddish head, feeding in old roots.- — Rough Osmoderma (Osmoderma scabra), p. 305. Trunk, Branches and Twigs: (a) A snout beetle gnawing the twigs and fruit. — Imbricated Snout Beetle {Epiccerus imbricatus) . {b) A small beetle boring in the branches just above a bud, and burrowing downward. — Apple Twig Borer {Amphicerus bicaudatus), p. 327. (c) A flattened grub tunneling in the bark and sap-wood; beetle bronzy metallic. — Divaricated Buprestis {Dicerca divaricata). (d) Large sucking insect with transparent wings, inflicting wounds on the smaller limbs and depositing eggs therein in August and September. — Dog-day Cicada {Cicada tibicen), p. 157. (e) Small circular scales, black in winter, with a circular depression about a central nipple. — San Jose Scale {Aspidiolus perniciosus), p. 126. {{) Dirty nests inclosing a colony of yellow caterpillars one-half inch long at end of twigs. — Cherry-tree Tortrix {Caccecia cerasivorana), p. 230. Leaves: (a) A small beetle feeding on the leaves of red cherry. — Cherry Leaf Beetle {Galerucella clavicollis) , p. 311. {b) A shiny, dark-green slug, one-half inch long, feeding on soft tissues, leaving the veins. — Pear or Cherry Slug {Eriocampoides limacina), p. 348. (c) Shining black plant-lice infesting the terminal twigs chiefly, which become distorted and discolored. — Cherry Plant-louse {Myzus cerasi), p. 144. {d) Large bluish-green caterpillar two inches long with blue warts on each segment, and coral red ones on the third and fourth segments. — Promethea Moth {Callosamia promethea), p. 180. (e) Large pale-green spiny caterpillar, striped on each side with white and lilac. — lo Moth {Hyperchiria lo), p. 180. (/) Caterpillars in colonies protected by webs in forks of branches in spring. — American Tetit-cater pillar {Malacosoma americana), and Forest Tent- caterpillar {M. disstria) not in webs, p. 203. {g) Caterpillars in colonies protected by webs covering the leaves in summer and early autumn. — Fall Web Worm {Hyphantria textor), p. 181. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS S;^ Fruit: (a) A crescent cut on the cherry; grub, white and footless, with a brownish horny head, feeding within. — Flum Curculio {Conlrachelus nenuphar), p. 329. (ft) Yellowish-white maggots feeding on the pulpy juices near the pit, inducing a rotting. — Cherry Fruit Flies {Rhagolctis cingulata and R. fausta), p. 265. XII. INSECTS INJURIOUS TO THE PEACH Root and Loiver Trunk: {a) Tunneling in the bark and sapwood of the root and lower trunk, causing an exudation of gum, which is seen at base of tree mingled with the castings. — Peach Tree Borer {Synanthedon exitiosa), p. 216. Trunk and Branches: (a) In early spring a minute caterpillar bores into the shodts of new leaves, killing the growing terminals. — Peach Twig Borer {Anarsia lineatella), p. 215. {b) Black hemispherical scales attached to the bark. — Peach Leaf Lecanium (Lecanium nigrofascialum) , p. 129. (c) A beetle eating the buds and gnawing into the base of the twigs, causing them to break and fall.- — New York Weevil {Ithycerus noveboracensis). (d) Round scales, gray or black; twigs presenting a scurfy appearance. — San Jose Scale (Aspidiotus perniciosiis) , p. 126. (e) Oval scars and longitudinal slits on bark produced by a green buffalo- shaped bug. — Buffalo Tree Hopper {Ceresa bubalus), p. 157. Leaves: (a) Plant-lice, living in colonies under the leaves, causing them to thicken and curl. — Peach Tree Aphis (Myzus persicce), p. 144. (6) Minute round scales located usually along the veins. — San Jose Scale {Aspidiotus perniciosus), p. 126. (c) Caterpillars protected." 1. In a tortuous tube. — Leaf Grumpier (Mineola indiginella), p. 213. 2. In folded leaves. — Oblique Banded Leaf Roller {Cacoecia rosaceana), p. 230. Fruit: (a) Long-legged yellowish beetles eating holes in half-grown peaches. — Rose Chafer (Macrodactylus subspinosus), p. 305. {b) Large yellow hairy beetles eating holes in ripe peaches.- — Bumble Flower Beetle (Euphoria inda), p. 305. (c) Small snout-beetles making a puncture and crescent in the young fruit. — Plum Curculio (Conotrachelus nenuphar), p. 329. XIII. INSECTS INJURIOUS TO THE RASPBERRY AND BLACKBERRY Roots and Base of Canes: (a) Large grub over two inches long, boring large tunnels in the woody portion of main root. The canes suddenly die. — Giant Root Borer {Prionus laticollis) , p. 321. 84 ECONOMIC ENTOMOLOGY (/)) Canes at base of main root girdled by a yellowish- white caterpillar in late summer and autumn. — Bramble Croiun Borer (Bembccia marginala), p. 218. Canes: (a) Longitudinal row of punctures on canes. — Black-horned Tree Cricket {QLcan- thiis nigricornis), p. 116. {b) Tips of raspberry canes wilting in early summer, due to a girdling of the canes inside the bark. — Raspberry Cane Maggot {Phorhia rubivora), p. 277. (c) Tips of shoots of raspberry wilting in July and August; two rows of hori- zontal punctures one inch apart at base of wilted portion, with a small hole between. Canes burrowed to the base before autumn. — Raspberry Cane Borer (Oberea bimaculala), p. 321. {d) Swellings on canes of raspberry and blackberry. — Red-necked Cane Borer (Agrilus^ruficollis), p. 301. Buds: {a) A small snout-beetle puncturing the flower stem close to the buds, and also the buds. — Strawberry Weevil {Anlhonomus signatus), p. 232. {b) A small yellowish beetle eating the flower buds, which either fail to open or wither. — Pale Brown Byturus {Bytiirus unicolor), p. 292. (c) A small brownish caterpillar eating the opening buds. — Bud Moth (Tmeto- cera ocellana), p. 225. Leaves: (a) Bugs sucking the sap of young growing parts, and arresting their develop- ment. — Tarnished Plant Bug (Lygus pratensis), p. 163. {p) Suckers and leaves curled up with enclosed lice. — Bramble Flea Louse (Trioza tripunctata), p. 152. (c) Small greenish larvae with spiny tubercles eating the leaves in spring. — Raspberry Saw-Fly {Monophadnus rubi), p. 347. Fruit: (a) A looper feeding on fruit of raspberry and blackberry. — Raspberry Geometer (Synchlora aerata). XIV. INSECTS INJURIOUS TO THE GOOSEBERRY AND CURRANT Canes: (a) Tips of canes girdled and wilted; pith tunneled. — Currant Stem Girdler {Janus integer), p. 345. (b) Centre of cane tunneled by a white caterpillar. — Imported Currant Borer {Synanthedon tipulijormis), p. 217. (c) Small flat circular scales, black or gray, with a depressed ring about a central nipple in black forms. — San Jose Scale {Aspidiotus perniciosus) , p. 126. {d) Oval hemispherical scales. — Currant Lecanium {Lecanium ribis). (e) Longitudinal rows of punctures on canes. — Black-horned Tree Cricket {CEcanthus nigricornis), p. ii6. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 85 Leaves: (a) Larvae, 20-Iegged, dull white when young, then greenish with black spots, finally greenish yellow, eating holes in the leaves in early spring. — Imported Currant Worm (Pteronus ribesii), p. 346. {b) Leaves curled, blistered, and with a reddish appearance on upper surface, caused by yellowish plant-lice — Currant Plant-louse {Myzus ribis), p. 145. (c) Leaves turning brown and dying. — Four Lined Leaf-hug {Poecilocapsus Uneatus), p. 163^ {d) Measuring worm feeding on leaves of gooseberry and black currant. — Currant S pan-worm {Cymatophora ribearia), p. 206. (e) White spots on leaves, produced by a pale green sucking insect occurring on the under surface. — Currant Leaf Hopper {Empoasca), p. 155. (/) Green plant-lice. — Green Gooseberry Aphis {Aphis sanborni). Fruit: (a) Greyish caterpillar boring into young fruit and eating out its contents. — Gooseberry Fruit Worm {Zophodia grossularia). (b) Purplish spots surrounding small circular scales. — San Jose Scale {Aspidiotus perniciosus) y p. 126. (c) Yellow oval maggots eating the gooseberry. — Gooseberry Midge (Cecido- myia grossularia) . (d) Small white maggot eating the currant and gooseberry, causing the fruit to turn red and fall. — Currant Fruit-miner (Epochra canadensis), p. 265. XV. INSECTS INJURIOUS TO THE GRAPE (Consult Bull. 33i> N. Y. Ag. Exp. St. and Farmers' Bull. 70, U. S. Dep. Ag.) Roots: (a) Producing soft yellow irregular spherical galls on rootlets and larger roots, causing death. — Grape Vine Phylloxera (Phylloxera vasfatrix), p. 148. (b) Large borer, cutting a tube through the root near the surface. — Broad- necked Prionus (Priontis laticollis). (c) Grub eating the bark of both the large and small roots. — Grape Vine Fidia (Fidia viticida), p. 311. Branches: {a) Young shoots suddenly break off or droop in spring; a small hole just above the base of the shoot leading into a burrow. — Apple Twig Borer (Amphicerus bicaudatus), p. 327. (b) Canes show roughened longitudinal rows of perforations in the bark. — Tree Cricket ((Ecanthus nigricornis), p. 116. (c) Canes exhibiting white cottony masses attached to a reddish-brown scale. — Cottony Scale {Pulvinaria vitis), p. 130. Leaves: {a) Leaves riddled with irregular holes about mid-summer by a little beetle. — Grape V tne Fidia {Fidia viticida), p. 311. 86 ECONOMIC ENTOMOLOGY (b) Small, shining, blue beetle boring into buds in spring, also eating small holes in expanding leaves. — Grape Vine Flea Beetle {Haltica chalybea),p. 315. (c) Long-legged brownish beetles eating the blossoms, leaves and fruit. — Rose Chafer (Macrodactylus suhspinosus), p. 305. {d) Greenish caterpillar, feeding within a folded leaf and skeletonizing it, about mid-summer. — Grape Leaf Folder (Desmia funeralis). (e) Leaves blotched and scorched, finally curling up and falling, caused by little jumping insects. — Grape Thrips or Leaf Hopper {Typhlocyba comes), P- 155- (/) Large greenish caterpillar, with a pale yellow stripe down each side and a horn near tail. — Grape Vine Sphinx {Ampelceca myron), p. 178. ig) Several other sphingid larvas feed on the leaves of the grape. {h) Black beetle eating the tissues on the upper surface of the leaves, and discoloring them. — Red-headed Sysiena {Systena frontalis), p. 315. (?) Producing small, irregular, spherical galls on the lower surface of the leaves. — Grape Vine Phylloxera (Phylloxera vastatrix), p. 148. (j) Large reddish-yellow beetle with six black spots on wing cover, eating holes in leaves. — Spotted Pelidnota (Pelidnota punctata), p. 302. Fruit: (a) Ripening fruit discolored and burrowed by a whitish caterpillar. — Grape Berry Moth [Polychrosis viteana), p. 228. (6) Holes eaten in ripe fruit; beetle large, yellowish, hairy. — Bumble Flower Beetle (Euphoria inda), p. 305. (c) Holes eaten in young fruit by a long-legged beetle. — Rose Chafer (Macro- dactylus subspinosus], p. 305. XVI. INSECTS INJURIOUS TO THE STRAWBERRY Roots : (a) A pinkish caterpillar boring irregular channels through the crown and larger roots, causing them to wither and die. — Strawberry Root Borer (Anarsia lineatella), p. 215. (b) A white grub boring downward from the crown. — Strawberry Crown Borer (Tyloderma fragarice), p. 332. (c) A large white grub eating the roots. — May Beetle (Lachnosterna sp.), p. 302. (d) Grubs girdling the roots, causing death. — Strawberry Root-weevil (Otio- rhynchus ovatus), p. 336. Leaves: (a) Brownish caterpillars, in June and August, rolling the leaves into cases and fastening them with silk. — Strawberry Leaf Roller (Ancylus comptana), p. 232. (b) Young plants gnawed off at the surface. — Cutworms, p. 185. (c) Small pale spotted active beetles riddling the leaves with holes in June. — Spotted Paria (Paria 6-notala). (d) Small active jumping striped beetles, eating holes in the leaves. — Striped Flea Beetle (Phyllotrela vittata), p. 314. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 87 (e) Twenty-legged grubs eating holes in the leaves. — Strawberry Saw fly {Entphytiis maculatus) Fruit: (a) Caterpillars feeding on the berry. — Stalk Borer (Papcipertia nitela), p. 196. (b) Minute black bugs producing a buggy odor when eaten with berry. — Flea- like Negro Bug {Corimelana pulicaria), p. 167. (c) Flower buds drooping and bending over. — Strawberry Weevil (Anthonomus signatus), p. 332- (d) Fruits deformed to "buttons. " — Strawberry Thrips (Euthrips Irilici), p. 122. XVII. INSECTS AFFECTING SHADE TREES (Consult Insects Affecting Park and Woodland Trees by Felt) (a) Feeding on the leaves. (b) Feeding or resting under webbed tents. (i) Hairy yellowish-brown and black marked caterpillars feeding on leaves within webbed tents in July-Sept.; adult moths white or black-spotted. — Fall Web Worm {Hyphantria cimca), p. 181. (2) Hairy black caterpillars, white stripe along middle of back, lateral white and yellow line with blue spots. Resting in silken webbed tents at angles of branches. — Orchard Tent-caterpillar {Malacosoma americana), p. 203. ^bb) Feeding free on the leaves. I. Adult mothsnot white. (i) Caterpillars with a broken line of white dots along back, and resting in masses on sides of branches and trunks, not within webs. — Forest Tent-caterpillar {Malacosoma disstria), p. 204. (2) Caterpillars with red heads and yellow and black tufts and pencils. Female moth wingless. — White-marked Tussock Moth {H enter ocani pa leucostigma), p. 202. (3) Brownish caterpillars with blue and reddish warts; hibernat- ing as egg-masses covered with hair; adult female moth with white wings marked with dark wavy lines, wings of males light brown. — Gipsy Moth {Porthetria dispar), p. 200. (4) "Measuring worms" feeding in the daytime in spring and early summer. — Fall Canker Worm {Alsophila pometaria), p. 205. (5) Caterpillars with tufts of white, black, or yellow hairs, and pencils of black or orange or white hairs. Feeding on hickory, butternut, etc. — Tiger Moths (Halisidota spp.), p. 183. (6) Caterpillars with sharp pale yellow hairs and with a pair of long black hair pencils on the first and third abdominal segments, and a single one on the eighth. Feeding on elm, maple, hickory, oak, ash, poplar, etc. — American Dagger Moth {Acronycta americana), p. 198. 58 ECONOMIC ENTOMOLOGY (7) Caterpillars black with a loose covering of soft whitish hairs. Feeding in clusters on walnut, hickory, oak, beech, etc. — Walnut Caterpillar {Datana integerrima), p. 199. (8) Small green caterpillars, skeletonizing the leaves of birches and forming small round white moulting cocoons on the twigs and leaves. — Birch Leaf Skeletonizer {Bucculatrix canadensisella), p. 236. (9) A bright yellow looper with rust-colored head and with ten crinkled black lines along the back. Attacks elm, basswood, hickory, apple, etc. — Lime-tree Winter Moth (Erannis liliaria). 2. Adult moths white. (i) Caterpillars reddish-black with only two pairs of prolegs; with three pairs of small tubercles on back; hibernate as egg- masses of 20-100 on branches. — Snow-white Linden Moth {Ennomos subsigniarius), p. 206. (2) Dark brown caterpillars, with a lateral row of white hairs and bright red tubercles on sixth and seventh adbominal seg- ments; hibernate as one-fourth grown caterpillars in nests of webbed leaves on tips of trees; adult moth with a tuft of brown hairs at tip of abdomen. — Brown Tail Moth {Euproctis chrysorrhcea), p. 200. 3. Adults are butterflies. Caterpillars large, black, red-marked and spiny, feeding in clusters on terminal branches of elm, willow, poplsiT.— Spiny Elm Caterpillar {Aglais antiopa). p 176. 4. Adults are beetles. Adults eating irregular circular holes in elm leaves and grubs skeletonizing the under surface. — Elm Leaf Beetle (Galerucella luteola), p. 309. 5. Adults are Saw-flies. (i) Larvae cylindric, coiled, yellowish-white, with a black line down the middle of back, feeding on elm, poplar, willow, etc. — Elm Saw-fly {Cimhex amcricana), p. 347. (2) Larvae with jet black head and green body, each segment except second marked with double parallel rows of dark dots; feeding on larch leaves. — Larch Saw-fly (LygcBonematus erichsonii), p. 346. (aa) Boring in trunks and branches. (b) Adults are moths. 1. Whitish caterpillars with distinct spots and tubercles making burrows in twigs and larger branches, which often die and project above leafy branches. Moths are white with blue and black markings. — Leopard Moth {Zeuzera pyrina), p. 237. 2. Large white or reddish- white caterpillars making large round irregular borings in oak, maple and locust. Moth is large, dark grey. — Carpenter Worm {Prionoxystus robinia), p. 238. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 89 (bb) Adults are beetles. 1. Long-horned or cerambycid beetles. (i) Large fleshy legless grubs making broad shallow tunnels in sapwood of sugar-maples, often killing limbs. Adult beetle brilliantly marked with yellow and black. — Sugar Maple Borer {Plagionotiis speciosus), p. 323. (2) A whitish hairy grub making a central burrow plugged with sawdust, and cutting off twigs of maple or oak. — Tivig Primer (Elaphidion villosum), p. 323. (3) White flattened legless grubs working under the bark of elm; adult a gray beetle with red lines and black spots. — Elm Borer (Saperda tridentata), p. 321. (4) White legless grubs making large irregular channels in sap- wood and inner bark of poplar; large blackened swollen scars on the surface of the trunk and limbs of affected trees. — Poplar Borer {Saperda calcarata) tunnels in poplar producing rough discolored scars on the trunk. Saperda Candida bores into hawthorn, mountain ash, and fruit trees, and Saperda veslita into basswood. (s) Club-shaped grubs, making irregular ugly scars opening into burrows in black locust. Adult beetle is dull black brightly marked with golden yellow, and feeds on golden rod blossoms. — Locust Borer (Cyllene robinice), p. 321, 2. Metallic wood borers or Buprestid beetles. (i) Large headed flattened legless grubs making shallow tunnels. — Flat-headed Borer (Chrysobothris femorata), p. 300. (2) A flattened whitish grub with a large flattened head, making irregular spiral burrows in the inner bark of birch. — Bronze Birch Borer {Agrilus anxhis), p, 301. {aaa) Sucking the juices from twigs or leaves. ib) On the leaves. 1. Producing terminal galls on white and Norway spruce; branch scraggly deformed. — Spruce Gall Aphis {Chermes similis), p. 150. 2. Producing galls on white and Norway spruce, not terminal, pine- apple shaped. — Spruce Gall Aphis (Chermes abietis), p. 149. 3. Snow-white woolly plant-lice on leaves of larch. — Larch Woolly Aphis {Chermes strobilobius). [bb) On the bark. 1. Clusters of woolly aphis on elm. — Woolly Aphis of Elm {Schizoneura americana), p. 145. 2. Reddish woolly bordered bark-lice on under surface of elm leaves. — Elm Bark-louse (Gossyparia spuria), p. 130. 3. Cottony masses attached to brown scales on under side of twigs of soft maple, elms, etc. — Cottony Maple Scale {Pulvinaria vilis), p. 130. 90 ECONOMIC ENTOMOLOGY 4. Hemispherical reddish scales mottled with black lines on under side of branches of maples. — Terrapin Scale (Lecanium nigrofas- cialum), p. 129. 5. Flocculent white masses upon greenbark of cultivated white pine. — Pine Bark Aphis (Chermes pinicorticis), p. 150. 6. Twigs of balsam twisted and leaves curled by plant-lice. — Balsam Twig Aphis {Mindarits abietinus). XVIII. INSECTS INJURIOUS TO GREENHOUSE PLANTS (a) Minute active white four-winged flies living on the under side of leaves, sucking the juices; young are oval, flat and greenish. — White Fly (Aleyrodes vapor- ariorum), p. 151. (6) Small soft mealy-covered bugs, with eggs enclosed in cottony sacks. — Mealy Bugs (Pseudococcus spp.), p. 131. (c) Oval, flat or saddle-shaped scales, on leaves of lemons, ferns, oleanders, crotons, etc. — Soft Scale (Lecanium hemisphericum), p. 134. {d) Round scales on leaves and twigs of ivy, date palms, etc. — Hard Scale {Aspidiotus spp.), p. 134. (e) White scales on leaves of Boston fern, aspidistra, etc., causing spotting and browning. — Aspidistra Scale {Hemichionaspis aspidistrcB), p. 135. (/) Green plant-lice, often infesting violets and sucking the juices from the leaves, checking the growth. — Green Aphis (Myzus persicce), p. 144. (g) Black plant-lice sucking the juices of chrysanthemums. — Black Aphis (Macro- siphum sanborni), p. 149. (A) Red mites, spinning fine webs on under surface of leaves and sucking the juices rendering the leaves sickly yellow.— i?e^ Spider (Tetranychus bimaculatus). (i) A small maggot, causing the edges of violet leaves to curl and turn yellow. — Violet Gall-fly (Diplosis violicola). (j) A small greenish-white and striped caterpillar, eating lower epidermis of chrysanthemums, cinerarias, roses, carnations, etc., and tying the leaves together. — Greenhouse Leaf-tyer (Phlyctcenia ferrugalis), p. 210. (k) Maggots feeding in flower and leaf buds of greenhouse roses, causing them to brown, blacken and die. — Rose Midge (Dasyneura rhodophaga), p. 248. (/) Flesh-colored legless grubs attacking roots of cyclamen, gloxinia, primula. — Cyclameti Borer {Otiorhynchus sidcatus), p. 336. XIX. INSECTS AFFECTING DOMESTIC ANIMALS (Consult Insects Affecting Domestic Animals by Osborn, Bull. 5, U. S. Div. Ent.) A. Sheep (a) Maggots in nostrils and in nasal sinuses, causing catarrh and staggers; deposited by a two-winged fly in June and July. — Sheep Bot-fly (CEstrus ovis). (b) Wool falls off in patches and large scabs form on body with much itching due to a mite. — Sheep Scab {Psoroples communis), p. 366. IDENTIFICATION OF INSECTS INJURIOUS TO CROPS 91 (c) Brownish flattened tick-like insects sucking the blood; common on lambs in spring. — Sheep Tick (Melophagiis ovinus), p. 279. B. Cattle (a) Swellings or "warbles" along the back in winter; bee-like flies bothering cattle in June and July. — Ox-warble {Hypoderma linealum and H. bovts), p. 255. (b) Small flies clustering on base of horns, flanks and belly of cattle in summer, causing them much annoyance. — Horn Fly {Hcemalobia scrrata), p. 272. (c) Slaty-colored sucking lice, often abundant on neck and shoulders of neglected cattle. — Short-nosed Ox Louse {Hcematopinus etiryslernus), p. 000. Long-nosed Ox Louse {Hamatoplnus vituli), p. i6g. (d) "Little red lice" feeding on the rough parts of the skin and on the hairs, causing irritation; most abundant in spring. — Biting Cattle Louse (Trichodectes scalaris), p. 100. (e) Hair falls off in patches and large scabs form — with much itching^due to mites. Common Cattle Scab Mites (Psoroptes Communis bovis), Sarcoptic Scab Mite (Sarcoptes scabiei bovis), Tail Mange Mite (Chorioptes bovis bovis). (See Farmers' Bull. 1017, U. S. Dep. Ag.). C. Horses (a) Bots attached to wall of stomach — adult fly light brown; does not bite but horse is worried; eggs laid on hairs of legs and shoulders. — Horse Bot-fly (Gastro- philus intestinalis) , p. 258. (b) Similar to (a) but eggs are attached to hairs of lips and nostrils. — Chin Bot-fly (Gastrophilus nasalis) and the Red-tailed Bot-fly (G. hcemorrhoidalis) , p. 259. (c) Large black fly that flies swiftly and bites severely, giving much annoyance to horses. — Horse Gadfly (Tabanus atratus), p. 252. D. Hogs (a) Gray sucking lice, often quite large. — Hog Louse (Hmnatopinus urius), p. 169. E. Poultry (a) Yellowish or reddish mites infesting hens and chicks at night; piercing the skin and sucking the blood, causing much irritation and often death. — Chicken Mite (Dermanyssus gallincB), p. 364. {b) Small pale yellow active insects feeding on rough parts of skin and bases of hairs and feathers, causing much irritation. — Common Hen Louse (Menopon pallidum), p. 100. (c) Minute mites burrowing under the scales of foot, leg, comb and beak, pro- ducing "scaly leg" with much irritation. Contagious. — Itch Mite (Sarcoptes mutans), p. 365. (d) Small mites causing the feathers to break off. Contagious. — Depluming mite {Sarcoptes gallince). 92 ECONOMIC ENTOMOLOGY XX. INSECTS OF THE HOUSEHOLD A. Annoying the Inmates (a) Slender two-winged insects; only the females bite or pierce the skin; larvae and pupae live in stagnant water. — Common Mosquito {Ctilex pipiens), p. 243. (b) Similar to (a) but larger and with wings spotted. — M alarial M osqiiito {Ano- pheles maculi pennis) , p. 244. (c) Two- winged insects, with four black lines on thorax; they lap but do not pierce; eggs laid on manure or decaying organic matter. — House Fly {Musca do- meslica), p. 270. {d) Similar to (c) but with six black lines on thorax, and with piercing mouth- parts. — Stable Fly (Stomoxys calcitrans), p. 271. (e) Compressed, wingless long-legged insects with piercing and sucking mouth- parts, hiding in bedding and clothing; eggs laid among hairs of cat or dog. — Cat and Dog Flea {Pulex serraticeps), p. 280. (/) Reddish-brown, flat bugs with buggy odor, hiding in day time in cracks, but active at night; with piercing and sucking mouth-parts. — Bed-bugs (Cimex Icclu- larius), p. 167. B. Feeding on or Destroying Clothing, Carpets, Upholstery, Etc. {a) Tiny dusky moths, laying eggs in furs or woolens, the larvae eating holes in them. — Case-making Clothes Moth {Tinea pellionella), p. 236. Webbing Clothes Moth {Tinea biselliella) , p. 237. Tapestry Clothes Moth {Trichophaga tapetzella), p. 237. {b) Small oval red, black and white beetles, whose grubs are hairy, feeding on carpets on underside, usually along a crack of the floor. — Buffalo Carpet Beetle {Anthrenus scrophularice), p. 291. (c) Tiny active wingless insects with silvery appearance, and with three long feelers at hind end of body, feeding on linen or paper containing starch, sugar, etc. Silver-fish {Lepisma saccharina), p. 95. C. Feeding on Food Products {a) Active wary light-brown insects with a "roachy" odor, found in pantries and bakeries; several species but the most common is the Croton-bug or German Cockroach {Ectobia germanica), p. 105. {b) Brown beetles, one-third inch long, whose grubs are brown above, white below and covered with long brown hairs; found where meats, skins and feathers are kept. — Larder Beetle {Dermestes lardarius), p. 291. (c) Large black flies with bluish abdomen and with black spines on thorax; eggs laid on meat. — Blow or Meat Fly {Calliphora vomitoria), p. 273. {d) Little red ants that have their nests in the wall or beneath the flooring. — House Ants {Monomorinm pharaonis), p. 361. (e) Black ants and pavement ants living outdoors sometimes invade houses. — Black Ants {Monomorium minutiim), p. 361. PART CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS THE COMMON ORDERS AND GROUPS OF INSECTS SYNOPSIS OF THE ORDERS OF INSECTS REFERRED TO IN THE CLASS BOOK Aptera Group. I. Thysanura. II. Collembola. Netiropteroida Group. Orthopteroida Group. Hemipteroida Group Dipteroida Group. I III. Plecoptera. IV. Ephemerida. V. Odonata. VI. Neuroptera. VII. Mecoptera. VIII. Trichoptera. IX. Mallophaga. X. Isoptera. XL Corrodentia. XII. Blattoidea. XIII. Mantoidea. XIV. Phasmoidea. XV. Dermaptera. XVI. Orthoptera. XVII. Thysanoptera. XVIII. Homoptera. XIX. Hemiptera. XX. Siphunculata. XXI. Lepidoptera. XXII. Coleoptera. XXIIL Diptera. XXIV. Siphonaptera. XXV. Hymenoptera. A. With two wings; mouth-parts formed for sucking or piercing; metamor- phosis complete.^ — DIPTERA (Flies). 93 94 ECONOMIC ENTOMOLOGY AA. With four wings. B. Mouth-parts formed for biting. C. Upper wings horny; metamorphosis complete. — COLEOPj'^j^ji (Beetles), p. 280. CC. Upper wings parchment-like; lower wings folded under the upper; metamorphosis incomplete. — ORTHOPTeROIDA Group (Locusts, etc.), p. 102. CCC. Upper wings membranous with many veins. — NEUROP- TEROIDA Group (Nerve-winged insects), p. 96. BB. Mouth-parts formed for sucking and biting; wings with few cross veins and similar in texture; metamorphosis complete. — HYMENOP- TERA (Bees, etc.), p. 343. BBB. Mouth-parts formed for sucking; wings covered with scales; metamor- phosis cora^\tie.—LEPI DOPTERA (Butterflies and moths), p. 169. BBBB. Mouth-parts formed for piercing. C. Beak jointed; palpi absent; last joint of tarsi not bladder-like. D. Wings of uniform texture; beak arising from the hinder edge of under side of the head; metamorphosis incomplete. —HOMOPTERA, p. 122. DD. Fore wings leathery at base, membranous at tip; beak arising from the front of the head; metamorphosis incom- plete.— Z^£M/Pr£i?J (True Bugs), p. 158. CC. Beak unjoin ted, palpi present; last joint of tarsi bladder-like, and without claws; wings similar; metamorphosis incomplete. — THYSANOPTERA (Thrips), p. 118. AAA. Wingless. B. Mouth-parts formed for biting; louse-like insects. C. Mouth-parts retracted within the head; no metamorphosis. — APTERA Group, p. 94. CC. Mouth-parts not retracted within the head. D. Antennas with many segments; metamorphosis incomplete. —CORRODENTIA (Book-lice), p. 103. DD. Antennas with not more than five segments; metamorpho- sis incomplete. — MALLOPHAGA (Biting-lice), p. 100. BB. Mouth-parts formed for sucking. C. Tarsus with a single hook-like claw; with a fleshy unjointed beak; parasitic on mammals (Parasitica). — SIPHUNCULATA, p. 167 CC. Tarsus five-jointed; body compressed; metamorphosis complete. — SIPHONAPTERA (Fleas). The Aptera Group Chief Orders and Families: A. Abdomen with at least 10 segments; antennae many-jointed; usually with terminal abdominal appendages. — Thysanura Order. B. Body covered with scales. — Lepismidce. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 95 BB. Body not covered with scales. C. Caudal appendages many-jointed. — Campodcidce. CC. Caudal appendages sickle-shaped. — Japygidce. AA. Abdomen with not more than six segments; antennae with not more than eight joints; no caudal appendages. — Collembola Order. B. Ventral spring present. C. Spring on penultimate abdominal segment. D. Abdomen globular. — Sminthuridce. DD Abdomen cylindrical. — Enlomobryidce. CC. Spring on antepenult abdominal segment. — Podurida. BB. Ventral spring absent. — Aphorurida. Of the above Apterous families only one, the LepismidcB of the Thysanura, contains forms that are of economic importance. ORDER THYSANURA LEPISMIDiE (Fish-moths) The Fish-moth, Silver Fish, or "SUcker" Linn.) sometimes does injury to books, papers, labels and starched clothing. It shuns light and is quite active. Adult. — A minute, glistening, scaly, fish- like active insect, wingless, 3^^ inch long, body tapering to hind end where are three long, bristle-shaped appendages; antennae prominent; coxae strongly developed; biting mouth parts. Another species, Lepismadomestica Pack., is found in bakeries and mills in some locali- ties. It has dusty markings on its upper surface and is 3-^ inch long. Control. — Frequent use of fresh insect powder, sodium fluoride, or a poison-bait of sweetened gluey paste and white arsenic on bits of cardboard. {Lepisma saccharina PODURID^ (Springtails) IT Fig. 50.— The silver fish {Lepisma saccharina) . {After Marlatt.) Two species may be noted in passing: Achorutes armatum sometimes attacking seedlings causing disfigure- ment and loss, and A. nivicola often abundant in maple sap in early spring. Both species are minute, and have some of the habits of flea-beetles (Fig, 51). 96 ECONOMIC ENTOMOLOGY The Neuropteroida Group Certain orders of aquatic insects have a superficial resemblance of wing venation, and were formerly grouped together into one order, the Neuroptera. Of the six main Orders three have incomplete metamorphosis, viz., Plecoptera, Ephemerida and Odonata, and three complete metamorphosis, viz., Tri- choptera, Neuroptera and Mecoptera. It is probable, therefore, that the first three orders are not so highly evolved as the last three. The former are lower than the Orthoptera, while the latter are higher and come between the Hemiptera and the Lepidoptera. Chief Orders: ^ The Neuropteroida (or nerve-winged) group of insects includes six main orders which may be sepa- rated as follows: A. Lower wings folded in plaits under the upper. B. Wings covered with hairs; tarsi 5-jointed ; metamorphosis complete. — Trichoptera (Caddice-fiies) . BB. Wings not covered with hairs. C. Tarsi 5-jointed; wings equal and with many veins and cross-veins; mouth-parts well developed; metamorphosis complete. — Neurop- tera (Dobson flies, Aphis lions, etc.). CC. Tarsi 3-jointed; hind wings larger than fore-wings; with caudal filaments; biting mouth-parts poorly developed; metamorphosis incomplete.- — Plecoptera (Stone-flies) (Fig. 54). AA. Lower wings not folded under the upper. B. Head prolonged into a beak; antennae long; metamorphosis com- plete. — Mecoptera (Scorpion-flies) . BB. Head not prolonged into a beak; antennae inconspicuous; metamor- phosis incomplete. 1 Handlirsch arranges these orders into groups as follows: Odonata Sub-class Libelluloidea. Plecoptera (Ephemerida) Sub-class Ephemeroidea. Plecoptera Sub-class Perloidea. Neuroptera | Megaloptera [ Sub-class Neuropteroidea. Raphidioidea J Panorpatae ) Trichoptera [ Sub-class Panorpoidea. Lepidoptera Fig. si. — The snow flea {A chorules nivi- cola). Enlarged greatly. {After Folsom.) CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 97 C. Abdomen with 2 or 3 long filaments; lower wings much smaller than upper; antennae short.^ — Ephcmcrida (May-flies) (Fig. 53).. CC. Abdomen without jointed filaments; wings about equal in size; antennas short. Odonata (Dragon-flies). The larvae of most of the Neuropteroid insects are aquatic and are of little economic importance in agriculture. They are of importance, however, in fish- culture. In the Stone-flies Newcomer has recently reported that several species of Taniopteryx (especially T. pacifica) with well developed mouth-parts cause consider- able injury to foliage and fruit in Central Washington. Fig. 52.- -M ay-fly {Hexagenia), adult. {After Folsom.) Fig. 53. — May-fly, nymph. LARVAL FORMS OF THE NEUROPTEROIDA A. Body cylindrical, caterpillar-like. — Mecoptera. AA. Body more or less depressed, not caterpillar-like. B. Mandibles united with corresponding maxiUte. — Netiroptera. BB. Mandibles separate from corresponding maxillae. C. Body encased in a shell of gravel, etc. — Trichoptera. CC. Body not encased in a shell. D. Abdomen with external lateral gills and terminated by 2 or 3 long gill processes. — Ephemerida (Fig. 53). 7 98 ECONOMIC ENTOMOLOGY DD. Abdomen without external lateral gills. E. X-ower lip strong extensile and furnished with a pair of opposable hooks; abdomen terminated by 3 leaf-like tracheal gills, or with 5 spine-like appendages. — Odonata. EE. Lower lip not extensile and without hooks; caudal filaments and antennae long and slender; thorax with 3 pairs of tracheal giWs.—Plecoptera. On account, however, of their common occurrence the economic entomologist should know a little at least regarding their habits and life-history. Stone-flies (Plecoptera). — The nymphs hve under stones in swift streams, are flattish, and have tracheal gills, long legs, cerci and Fig. 54. -An adult stone-fly {Pteronarcys regalis). Folsom). Slightly reduced. {After antennae. The adults are greyish and have prominent wings. The hind wings are the larger and when at rest are folded under the front ones. The larvae furnish food for fishes (Figs. 54 and 55). May-flies (Ephemerida). — May-flies are well-known insects, being attracted to lights in immense numbers in early summer. They have large delicate wings and 2 or 3 long caudal filaments. The fore wings are much larger than the hind ones. The nymphs Hve at the bottoms of bodies of water, and have long legs, caudal filaments and prominent tracheal gills. They_mature in i to 3 years, and furnish abundant food for fishes. CLASSIFICATION AND DESCEIPTION OF COMMON INSECTS 99 Dragon-flies and Damsel-flies (Odonataj.- — These insects are also well known. They are rapid fliers over bodies of water, feeding on flies and mosquitoes. The nymphs live at the bottom of ponds and streams. They have long legs, and are flat and spiny. Dragon-flies hold their wings horizontally when at rest, and the nymphs have rectal respiration; while the damsel-flies hold their wings vertically when at rest, and the nymphs have three caudal tra- cheal gills (Fig. 56). Caddice-flies (Trichoptera). — The larvae of these insects are known as caddice-worms, and live in water within protecting cases of fine gravel, leaves, sticks, stalks or small shells, •fastened together by threads of silk. They crawl about carrying their cases with them. When full-grown they change to pupcB within the cases and at length emerge as four-winged flies. During summer immense numbers are attracted to lights at night. The wings are hairy, and, at rest, are held like a roof over the back, usually laid on water plants. Fig. 55. — Nymph of s t o n e-fi y {Pteronarcys regalis). The eggs are Fig. 56. -Dragon-fly {Libellula pulchella). Last nymphal skin and wings. Slightly reduced. {After Folsom.) Dobson-flies, Lace-wings, Ant-lions (Neuroptera). — Dobson-flies are large insects with prominent biting mouth-parts and wings. Their larvae live under stones in swift streams, and have rather conspicuous tracheal gills. They become full-grown in about three years. lOO ECONOMIC ENTOMOLOGY Lace-wings are delicate pale-green insects with finely veined wings. The larvae have large jaws, and owing to their habit of feeding upon aphids are called aphis-lions. The pupae are enclosed in a white cocoon of silk (Fig. 57). Ant-lions are predaceous larvae, which lie in wait for their prey at the bottom of funnel- shaped pits. The adults have narrow delicate wings. {Chrysol''a)7%\St^rl Scorpion-flies (Mecoptera) —Scorpion-flies duced. {After Folsotn.) have their head prolonged into a beak. The larvae live in the ground and are caterpillar- like. Both larva and adult are carnivorous. ORDER MALLOPHAGA (BITING LICE) Chief Families and Genera: A. Antennae filamentous, exposed, 3- or 5-jointed; maxillary palpi absent; mandibles vertical; middle and hind segments of thorax fused. B. Antennas 3-jointed; tarsi with a single claw; infesting mammals. ■ — Trichodectidce. Genus: Trichodedes. BB. Antennae 5-Jointed; tarsi with two claws; infesting birds. — Philopteridce. Genera: Docophorus, Lipeurus, Nirmus, Goniodes, Goniocoles. A A. Antennae clavate or capitate, concealed, 4- jointed; maxillary palpi 4- jointed; mandibles horizontal; middle and hind segments of thorax sepa- rated by a suture. . B. Tarsi with a single claw; infesting mammals. — Gyropida. Genus: Gyro pus. BB. Tarsi with two claws; infesting birds. — Liotheidce. Genera: Menopon, Trinoton. (Consult Bull. 5, n.s. Divison of Etomology, U. S. Dept. of Agriculture, by Osborn) Although most commonly found on poultry, Biting Lice some- times infest the larger domestic animals. They do not suck blood but feed on the rough parts of the skin and at the base of hairs and feathers, causing considerable irritation. Young chicks frequently suffer severely from their attacks. The most abundant species found on fowls is the common hen louse (Menopon pallidum), a pale yellow active insect, 3^5 inch long, with six legs (Fig. 58). The eggs or "nits" are oval objects attached to the vanes and CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS lOI barbs of the feathers, usually on the down feathers. They hatch in 8 to lo days and become full grown in 2 to 3 weeks. Dampness, filth and warm weather favor their increase. Control. — (a) Sanitary surroundings with access to a dust bath. (b) Dusting with lice powder, such as insect powder, or one pre- pared as follows: 3 parts gasoline, i part crude carbolic acid (90- 95 per cent.), or i part cresol. Mix together and add, with stirring, plaster-of-Paris to take up all the moisture (about 4 qts. to i qt. of Hquid). (c) Dusting with sodium fluoride. All remedies should be applied more than once. Following are the common Mallophaga in- festing domesticated birds: A. Feather-lice Infesting Chickens: 1. Head nearly square, abdomen not con- spicuously marked, ^^^5 inch long. — Goniocotes hologaster Nitzsch (Lesser Chicken Louse). 2. Head almost circular in front, nar- rowed behind, thorax small; head, thorax, and legs yellowish; white stripes on segment of abdomen, 3^^ inch long. — Goniocotes abdominalis ^'^■ Piaget (Larger Chicken Louse). 3. Yellowish with black markings, uncommon. — Goniocotes hur- netti Pack. 4. Smooth and shining, head squarish, }{q inch long, tawny, pubes- cent. — Goniodes dissimilis Nitzsch. 5- Body elongated, smooth and shining, black margins. — Lipeurus variabilis Nitzsch. 6. Yellowish, slender louse, }io inch long, common. — Menopon pallidum Nitzsch (Hen or Chicken Louse). B. Feather-lice of Ducks and Geese: 1. Head and thorax red with dark bands; abdomen whitish at middle, brown at sides, 3^^ inch long. — Docophorus icterodes Nitzsch. 2. White, smooth, and shining, on goose. — Lipeurus tadornce Denny. 58. — Chicken louse. {Menopon.) I0 2 ECONOMIC ENTOMOLOGY 3. Large, 3^^ inch long, elongated, yellowish, head cone-pointed, on ducks, — Lipeurus squalidus Nitzsch. 4. Large well-marked louse, 3^^ inch long, on ducks. — Trinotum luridum Nitzsch. 5. White, almost transparent louse, on goose. — Trinotum lituratum Nitzsch. C. Feather-lice of Turkey: 1. Head with hind angles extending backward into bristly styles; ^^ inch long. — Goniodes stylifer Nitzsch. 2. Yellowish, elongated, flat pointed body, 3^7^ inch long. — Lipeurus poly trapezius Nitzsch. Orthopteroid Insects The old Order Orthoptera is now broken into several new Orders by the elevation of certain Families to ordinal rank. The relationship of these and other allied orders is shown by the following grouping: I. Sub-class: Orthopteroida. Orders: Orthoptera, Phasmoidea and the allied orders Dermap- tera and Thysanoptera. IL Sub-class: Blattaeformia. Orders: Mantoidea, Blattoidea and the allied orders Isoptera, Corrodentia and Mallophaga. Chief Economic Orthopteroid Orders: A. Hind femora large and fitted for jumping. — Orthoptera (Locusts, Crickets, etc. AA. Hind femora not large, not fitted for jumping. B. Body elongate; abdomen without movable forceps. C. Front legs spined and fitted for grasping.^ — Mantoidea {Mantids). CC. Front legs not formed for grasping, legs long and slender. — Phas- moidea (Walking slicks). BB. Body elongate; abdomen with movable forceps; fore wings short and horny, hind wings nearly circular. — Dermaptera (Earwigs). BBB. Body oval, flattened; legs fitted for running.- — Blattoidea (Cockroaches). ORDER ISOPTERA (WHITE ANTS) FamUy TERMITID.S This order is characterized by incomplete metamorphosis, biting mouth-parts and net-veined wings that fold flat upon the back. CLASSinCATION AND DESCRIPTION OF COMMON INSECTS I03 There is but one Family — the TermitidcB. The members of each species live in communities in the ground or sometimes on trees and include males, females and neuter workers and soldiers. They feed upon vegetable fibre, and are often injurious to furniture, books and wooden structures. Termites are most abundant in tropical or semi-tropical countries. A few species such as Leucotermes flavipes are found as far north as Canada. ORDER CORRODENTIA (BOOK-LICE) Family PSOCID^ These insects have biting mouth-parts and are either wingless or with roof-like wings. The Family PsocidcB includes the minute book-lice which are often injurious to old books, herbaria and insect collections. The most common species is Atropos divinatoria, a minute, pale-colored wingless insect. It feeds upon the paste of book bindings and upon decaying vegetable and animal matter. Control. — When severe infestations occur, fumigate with sulphur (2 lb. to 1000 cu. ft.) or with hydrocyanic acid gas. ORDER BLATTOIDEA (COCKROACHES) Family BLATTID.S Genera and Species: A. Last ventral segment of female abdomen plane not compressed; fore femora rarely provided with spines. B. Sub-genital stylets present in the males, upper wings of females short. — Ischnoptera. I. pennsylvanica brown, sides of pronotum yellow. BB. Sub-genital stylets absent in the males. Upper wings of both sexes long. — Blattella = Edohia = Phyllodromia. B. germanica (Croton bug), length )^ inch. A A. Last ventral segment of female abdomen compressed and divided; fore femora spined. B. Wing-covers not reaching tip of abdomen. — Blatta. B. orientalis (Oriental Cockroach). BB. Wing-covers reaching beyond the abdomen. — Periplaneta. C. Wing-covers much exceeding abdomen. — P. americana. CC. Wing-covers but little exceeding abdomen; a bright yellow stripe on basal half of their outer margin. — P. australasice. I04 ECONOMIC ENTOMOLOGY Several injurious species of cockroaches occur: (i) American Cockroach, (2) Austrahan cockroach, (3) Oriental cockroach, and (4) German cockroach or Croton Bug. I. American Cockroach {Periplaneta americanaL.), a native species, is a large dark brown insect i)-2 inches long, with well-developed wings in both sexes, 13^^-2 inches long; thorax with an obscure yellow border. Eggs held within a capsule until hatched. Duration of life-cycle about a year. Nocturnal. Fig. 59. — The oriental roach {Blalla orienlalis): a, female; b, male. All natural size. {After Marlalt, U. S. Bur. Ent.) 2. Australian Cockroach (Feriplanela australasia L.), ij^ inches long; resembles preceding but the yellow band on thorax is much brighter and more definitely limited. Upper wings have a dash of yellow on each side. Abundant in the south. 3. Oriental Cockroach {Blatta orientalis Fol.) or "black beetle," is a nearly wingless dark brown or black robust form, about an inch long— the male with wing cases one-half to three-fourths length of abdomen; female wingless. Notably gregarious and larger than the Croton Bug (Fig. 59). CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS I05 4. Gennan Cockroach or Croton Bug (Edobia germanica L.), has a light brown thorax marked with two dark brown stripes. Both sexes with well-developed wings. Active and wary, relatively small, ^8 inch long. All the roaches have a foetid roachy odor, and are said to feed on the bedbug (Fig. 60). They are particularly abundant in pantries, kitchens and bakeries and they feed on almost any kind of dead animal matter and cereal products. The eggs are produced in a brown cap- sule which is often carried about for a time before deposited in a crev- ice or nook. Control. — A bait of powdered borax mixed with sweetened chocolate; a trap of flour and plaster-paris and water; fumigation with hydro- pic. 60. — The German roach {Ectohia germanica) : a, first stage; b, second stage; c, third stage; d, fourth stage; e, adult; /, adult female with egg case; g, egg-case, enlarged; h, adult with wings spread. All natural size except g. {From Riley.) cyanic acid gas. Dust the runways or hiding places with sodium fluoride mixed with flour by means of a dust gun or blower. Boric acid is also effective. ORDER MANTOIDEA (PRAYING MANTIDS) Family MANTID.S The Praying Mantids are predaceous insects and for centuries have been looked upon as uncanny creatures both in the old and new worlds. The most common American species is Stagmomantis Carolina, but this form does not breed normally north of southern New Jersey, Pennsylvania and Ohio. In 1899, however, the European species Io6 ECONOMIC ENTOMOLOGY (Mantis religiosa Linn.) was found in New York State, and in 1914 in Ontario. The adult forms are elongated, with large grasping forelegs, long prothorax and a small transverse head. The eggs are laid in shingled masses on twigs, coated with a hard gummy substance. ORDER PHASMOroEA (WALKING-STICKS) Family PHASMID^E This Family is represented by the common Walking-stick insect {Diapheromera Jemorata, Say), a peculiar creature with long slender body and legs. The outer wings are either wanting or very short. Life-history. — The eggs are dropped singly in autumn from the shrubs and rest on the ground all winter among the leaves, hatching in early summer. The nymphs feed upon leaves, and reach maturity in late summer and early fall, when they resemble the twigs upon which they rest. Occasionally this insect becomes injurious on hazel and beech. ORDER DERMAPTERA = EUPLEXOPTERA (EARWIGS) European Earwig (Forficula auriculari a Linn.). — This insect is held in check in Europe by parasites and other natural agencies but the practical absence of these checks allows it to multiply rapidly in America wherever it has been introduced. At Newport, R. L, it is a serious pest of Lima-beans, dahlias, early roses, chrysanthemums, clovers, grasses, etc. The adult females hibernate in the soil, and the white eggs are laid in the soil. The nymphs are night feeders. They are white at first but gradually darken in color to a steel grey — 4 instars. Adults ap- pear about the middle of July. They are rich reddish brown with yellow brown wing-covers and legs; about ^^ inch long. The forceps is nearly straight in the female, but curved in the male. Control. — Use poison bait before July ist and spray plants with arsenate of lead; collect by traps. Labia minor Linn., also an adventive earwig from Europe, is widely distributed in U. S. and Canada. Not of economic importance. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS I07 ORDER ORTHOPTERA (LOCUSTS, GRASSHOPPERS AND CRICKETS) FAMILIES A. Antennse shorter than body.— Acridid(e (Locusts or Short-horned Grass- hoppers) . AA. Antennae longer than body. B. Tarsi 4-Jointed. — LocuslidcB {Long-horned Grasshoppers), BB. Tarsi 3-jointed. — Gryllidm {Crickets). AcRiDiD^ (Locusts or Short-Horned Grasshoppers) Sub-families, Genera and Species (Figs. 61-63). Sub-families: A. Pronotum extending over abdomen; claws of tarsus without pulvillus; size small. — Teltigince. ppH- cer -fq.pl oyp. Pig. 61. — Abdomen of female Melanoplus bivittatus. A, lateral view; B, dorsal view; C, central view; D, egg guide; au., the auditory organ; sp., spiracle; ovp., ovipositor; g.pl., genital plate; p. pi., podical plate; cer., cercus. {After Lugger.) AA. Pronotum not extending over abdomen; claws of tarsus with pulvillus; size larger. B. Prosternum with tubercle. — Acridince. BB. Prosternum without tubercle. C. Vertex and front of head meeting at an acute angle. — Tryxalincs. CC. Vertex and front rounded. — (Edipodina. io8 ECONOMIC ENTOMOLOGY Genera of the TeUigina: A. Antennae 12-jomted and pronotum rounded. — Batrachidea. A A. Antennae 13-14-jointed; pronotum horizontal. — Tettix. AAA. Antennae 22-jointed; pronotum horizontal. — Tettigidea. (For species see Blatchley's Orthoptera of Indiana.) Genera of the A cridince: A. Wings as long or longer than the abdomen. B. Pronotum sloping from median carina; extremity of abdomen in males not swollen. — Acrid ium or Schislocerca. BB. Pronotum flattened; extremity of abdomen in males swollen. — Melanoplus. Fig. 62. — -Abdomen of male Melanoplus hiviilalus. A, lateral view; B, dorsal view; C, ventral view. {After Lugger.) Species of Acridium: A. Size large; antennae rather short. — A. americana. AA. Size medium; antennae longer. B. Color yellowish-brown or olive-green. — A. alutacea. BB. Color rusty-brown; no yellowish stripe on dorsum. — A. rubiginosa. Species of Melanoplus: A. Apex of last ventral segment of male distinctly notched (Fig. 63) . B. Length of body to tip of wing-covers 29-35 mm. — M. spretus. BB. Length of body to tip of wing-covers 23-26 mm. — M. atlanis. A A. Apex of last ventral segment of male entire, or at least obscurely notched. B. Anal cerci enlarged at apex. — M. bivitlatus. BB. Anal cerci tapering. C. Species of medium size; anal cerci much narrowed, but without a notch. — M. femur-ruhrum. CC. Species of large size; anal cerci suddenly narrowed, making a prominent right-angled notch on lower side. — M. difereniialis. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS IO9 Genera of the Tryxalince: A. Foveolae of vertex present, and visible from above. Lateral carinas of pronotum incurved. — Stenobothrus curlipennis. AA. Foveolse absent; lateral carinas nearly parallel. — Chrysochraon conspersum. Genera and Species of QLdipodina: A. Wings with the disk yellow. B. Apical half of wing dusky. C. Dorsal aspect of head with a slight median carina which is quite prominent in the central foveola. — Enco ptolophus sordidus. CC. Dorsal aspect of head without median carina; central foveola less distinct. — Chortophaga viridifasciata. BB. With a dark band across the wings. — Spharagcmon (equate. A A. Wings with the disk black. — Dissosleira Carolina. AAA. Wings transparent with dark veins; tegmina smoky brown with darker spots and yellowish blotches on sides. — Camnula pellucida. Fig. 63. -Tip of male abdomen of Melanoplus, dorsal view. A, M . femur-rubrum; B, M. spretus; C, M. atlanis; D, M. differenlialis. In the West the Rocky Mountain Locust {Melanoplus spretus) did, and occasionally does, produce much injury to grain and other crops. Another species more widely distributed is M. atlanis which sometimes becomes migratory. The Red-legged Locust or Grasshop- per {M . femur-rubrum) , the Two-striped Locust {M. bivittatus) and the Pellucid Locust {Camnula pellucida) in the East and the Differential Locust {M. diferentialis) in the South are the species that do most injury. Red-legged Locust or Grasshopper {Melanoplus femur-rubrum, DeG.).^ — ^This locust is usually the most abundant form in the East, and is most numerous in low grounds and cultivated fields where vege- tation is more or less rank (Fig. 64). Adult. — Of medium size, about an inch long; reddish brown in color; tegmina sometimes without spots but usually spotted, surpassing the hind femora, which are reddish brown; hind tibiae red with black no ECONOMIC ENTOMOLOGY spines; cerci of male narrowing from tip to base and subgenital plate narrower at apex than at base. Fig. 64. — Red-legged grasshopper {Melanoplus fernur-r ubrum) : Above, adult male; below, adult female. About twice natural size. (After W. R. Walton, U. S. Bur. Ent.) x^ -^ , ^Wt VppP^^iipl 1 m. ^^^ '^H Hi 1 1 P -■ ^'-^'/'/MIw! m Fig. 65. — Locust ovipositing; egg pod in ground at right. Enlarged one-half. {After Gibson, Ent. Circ. 5, Dept. Agric, Ottawa.) Eggs. — Deposited in pod-like masses in the ground; oblong-oval. Nymphs. — Vary in size according to age and month; all stages of developing wings; grey to yellow; five moults. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS III Life-history. — Nymphs hatch from eggs in spring; these mature in August and September, when eggs are laid in the ground and over- winter there (Figs. 65 and 66). The Lesser Migratory Locust (Mela- noplus atlanis Riley). — ^A native Ameri- can species; often abundant in Eastern Canada, causing serious injury. Com- pared with M. femur-rubrum the fe- male has a yellow under surface, and more distinctly banded hind femora, and the male has the apex of the sub- genital plate notched, the cerci shorter and less tapering, and longer tegmina which are also more distinctly spotted. It has a distinct patch of black on the neck or collar. Egg deposition occurs from July to September. Mature forms appear from July ist, and are often abundant in open sandy regions with sparse vegetation. Fig. 66. — Egg pod of locust opened to show arrangement of eggs; individual eggs at side, natural size. {After Gibson, Ent. Circ. 5, Dept. Agric, Ottawa.) ^^ x!=*^N Pig. 67. — Lesser migratory grasshopper {Melanoplus atlanis): Above, adult male; below, adult female. About twice natural size. {After W. R. Walton, U. S. Bur. Ent.) The nymphs undergo five moults; the eggs are deposited in the ground in small pod-like capsules, and hatch in the spring (Fig. 67). 112 ECONOMIC ENTOMOLOGY Differential Locust (Melanophis diferentialis Uhler). — This locust is larger than those described above, about i3''^ inches long, and is dark brownish-green or olive-brown in color. The hind legs are yellow with black basal tibial ring and black spines. The subgenital plate short and broad, and the cerci of male boot-shaped. It is fond of the Greater Rag-weed. It is a southern form. Fig. 68. — Two-striped grasshopper {Melanoplus bivitlatus): Above, adult male; below, adult female. Twice natural size. {After W. R. Walton, U. S. Bur. Ent.) Two-striped Locust {Melanoplus hivittatus Say). — This locust is not so large as the Differential locust, being about i^^i inches long, and is dull olive-brown above and yellowish beneath. A narrow yel- lowish stripe runs along each side from the eye to the tip of the teg- men. The hind femora are yellow, and the hind tibiae coral red with CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS II3 black spines. The cerci of the male are stout, and two lobed; the subgenital plate is narrow. The young and newly transformed adults are greenish (Fig. 68). Its transformations are later than those of M. atlanis. Clear-winged Locust (Camnula pellucida Scudder). — This locust occasionally does serious injury' in the West, and frequents high dry soil. It is of a light brown color; the tegmina are smoky brown with darker spots and yellowish blotches on the sides and a yellowish brown stripe along each humeral angle. The wings are transparent and pellucid with dark veins. Body of male 19 mm. long, of female 22 mm. It is often associated with M. atlanis in the East, and is the earliest of the grasshoppers (Fig. 6g). ^e-^ Fig. 69. — Pellucid or clear-winged grasshopper {Camnula pellucida): Adult female. About twice natural size. {After W. R. Walton, U. S. Bur. Ent.) Carolina Locust {Dissosteira Carolina Linn.). — This locust is larger than the preceding species and is of a pepper-and-salt color, with varia- tions from grey to yellow or reddish. The hind wings are black margined with yellow. It is sometimes injurious to corn, wheat, alfalfa and soy beans. Natural Enemies of Locusts. — Robber-flies, bee-flies, flesh-fly and blow-fly larvae, digger wasps and bhster-beetle larvae; birds and domes- tic fowls; toads, snakes, moles, mice, ground squirrels, skunks and hogs; mites, spiders, "hair-snakes," etc. Control of Locusts. — (a) AppHcation of poisoned baits (see Part IV, p. 398). {b) Use of hopperdozers. {c) Destruction of eggs by fall cultivation, {d) Co-operation of communities. (Consult U. S. Com. Rept. or. Rocky Mt. Locust, 3 vols.. Farmers' Bulls. 691 and 747, U. S. Dept. Agr.; Giro, s, Ent. Br. Dept. Agr., Can.; Cornell Bull. 378; Mich. sp. Bui. 83) 114 ECONOMIC ENTOMOLOGY LocusTiD^ (Long-horned Grasshoppers or Locusts) More Common Genera and Species A. Wingless or with rudimentary wings and wing-covers. B. Pronotum not extended over meso- and metanotum. — Ceuthophilus. BB. Pronotum extended over meso- and metanotum. — Thyreonolus. AA. Winged. B. Tegmina expanded in the middle. C. Tegmina much broadened in the middle, concave. — Cyrtopkyllus. CC. Tegmina somewhat broadened in the middle, not concave. D. Ovipositor very small. — Microcentrum. DD. Ovipositor of medium size. — Aniblycorypha. BB. Tegmina not expanded in the middle. C. Vertex of the head with a conical projection forward. — Cotiocephalus. CC. Vertex of the head without a conical projection. D. Ovipositor straight or very nearly so; insect small. — Xiphidium. DD. Ovipositor curved; insect large. E. Ovipositor curved sharply upward. — Scudderia. EE. Ovipositor sword-shaped. — Orchelimum. Species of Ceulhophilus: A. Fore femora about as long as pronotum. — C. maculalus. AA. Fore femora longer than pronotum. — C. brevipes. Species of Thyreonolus: A. Pronotum well rounded behind. — T. dorsalis. AA. Pronotum nearly square. — T. pachymerus. The members of this family are seldom of sufl&cient importance economically to require special treatment. The katydids, shield- backed grasshoppers, cricket-like grasshoppers, and meadow grass- hoppers belong here and are interesting objects of study. Recently it was found that two species of katydids {Scudderia furcata Brunner and Microcentrum rhombifolium Sauss.) are injurious to oranges in California, often causing serious loss. (Bull. 256, Bur. Ent. U. S. Dept. Agr., 1915.) Gryllid^ (Crickets) Genera and Species A. Fore tibiae broad, fitted for digging (Fossorial Crickets). B. Insect small; antennae ten- to twelve-jointed. — Tridactylns. BB. Insect large; antennae many-jointed. — Gryllotalpa. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS II 5 AA. Fore tibiae slender. B. Hind femora stout (True Crickets). C. Last segment of the maxillary palpi of the same length as the next to the last. — Grylliis. CC. Last segment of the maxillary palpi double the length of the next to the last. — Nemobius. BB. Hind femora slender (Tree Crickets).- — CEcanthus. Specks of Cryllus: A. Black field crickets. B. Ovipositor 13-14 mm. long; male more slender. — G. pennsylvanicus . BB. Ovipositor 18 mm. long; male stout. — G. ahhrevialus. AA. Straw colored house crickets.— '25 inch long, elongate, thimble-shaped. Larva. — -A hairy black soft velvety caterpillar, 2 inches long, with a white stripe down the back; on each side a row of blue spots; sides streaked with white or yellow lines; under side blackish. Caterpillars of a colony form silken tents at angles of branches and feed away from tents. Matures in 4-5 weeks. Pupa. — Cocoons formed under bark, in crevices, etc., elongated- oval; outer silk delicate and loose, inner part firm and close; a yellow powder within. Pupal stage lasts 2-3 weeks. Life-history. — -Winters in the egg state; eggs hatch in May when the buds are beginning to open and the caterpillars reach maturity in June. 204 ECONOMIC ENTOMOLOGY Adults appear and eggs are laid in July. There is but one brood each year. Forest Tent-caterpillar (Malacosoma disstria Hbn.) differs from the preceding in the following particulars: egg-mass is nearly square at the ends; caterpillars do not construct tents; line along the back is broken with dots; transverse lines on the wings of moth are darker than ground color. Parasites. — Pimpla conqiiisitor, P. inquisitor, Tachina mella, Anomolon exile. Calosoma and Podisus are predaceous enemies. Control. — Destroy the egg-masses; spray caterpillars with arseni- cal; burn off the tents; band trees with burlap or tar to prevent the caterpillars from ascending. GROUP GEOMETRINA (GEOMETERS) Chief Families (after Comstock) A. Media2 of the hind wings wanting, being represented merely by a fold in the wing. — Ennomidce. , AA. Media2 of the hind wings present. B. Mediaa of the hind wings arising much nearer to Mediai than to Medias. Wings usually green. — Gcometridce. BB. Media2 of the hind wings arising nearly midway between Mediai and Medias or nearer to Mediaj than to Mediai. Wings rarely green. C. Subcosta and Radius of hind wings extending distinctly separate from each other, except that they are connected by a cross vein near the middle of the discal cell. — Hydriomenida. CC. Subcosta and Radius of hind wings approximated or coalesced for a greater or less distance. D. Subcosta and Radius of the hind wings closely approximated but not coalesced along the second fourth (more or less) of the discal cell. E. Radius and Mediai of hind wings separating at or before the apex of the discal cell. — Ennomidce. EE. Radius and Mediai of hind wings coalesced for a considerable distance beyond the apex of the discal cell.— Alonocteniida;. DD. Subcosta and Radius of the hind wings coalesced for a short distance near the beginning of the second fourth of the discal cell, thence rapidly diverging. — Sterrhida. DDD. Subcosta and Radius of the hind wings coalesced to or beyond the middle of the discal cell. E. Fore wings with one or two accessory cells. — Hydriomenida. EE. Fore wings without an accessory cell. — Monodeniida. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 20$ MONOCTENIIDiE Spring Canker Worm {Palccacrita vcrnata Peck.). — A widely distrib- uted insect from Canada to Texas, and from Maine to Kansas and California. Adults. — ^Male moth with thin brownish-grey silky wings, i inch expanse; fore wings with a row of light markings near outer margin and three transverse dark irregular bands; female moth wingless, 3:3 inch long, dull grey or brown with a dark brown stripe down the middle of the back. April-May. Eggs. — Yellowish-green, oval, 1.^5 inch long; laid in irregular masses of about 50 under loose bark, in crevices. Hatch in a month about the time of unfolding of the leaves. Larva. — Slender, cylindrical, i inch long, with only two pairs of pro- legs, with narrow longitudinal yellow-white lines, and a yellow stig- matal stripe along each side; ventral surface white. Mature in 4 to 5 weeks, when it drops to ground by a silk thread and enters to a depth of 2 to 5 inches. Pupa. — Cocoon an earthen cell lined with silk; pupa remains in it until following spring; light brown and pitted. Male pupa spined. Parasites, Etc. — Hymenoptera, Diptera and birds. Fall Canker Worm (Alsophila pometaria Harris). — Widely distrib- buted^ — -Eastern Canada, New England, New York, Ohio, California. Adults. — Male moth with darker, stronger wings than that of the spring Canker Worm; fore wings crossed with two light bands; hind wings darker. Female moth wingless, ashy-grey, no markings, an- tennae long. October-November. Eggs. — Brownish-grey, flower-pot like, outer end with a dark spot surrounded by a dark ring; laid in clusters of 100, in rows, each egg fastened on end and to the bark. Hatch in May, about the time of unfolding of the leaves. Larva. — -Resembles in a general way that of the Spring Canker Worm, but has a broad dark stripe along the back and three pairs of prolegs near hind end of body. When disturbed or full grown it drops to the ground by a silken thread. It forms a cocoon in the ground. Matures in 4 to 5 weeks. Pupa. — Cocoon tough and contains more silk than that of Spring Canker Worm; pupa stouter and spine of male pupa forked. 2o6 ECONOMIC ENTOMOLOGY Control. — Spray with arsenate of lead just after the leaves unfold; band trees with burlap in fall. ENNOMIDiE Pepper-and-salt Currant Moth (Amphidasis cognataria Guen.). — Injures leaves of currant, gooseberry, plum, Spirea and maple. Adult. — Body grey, with black dots; wing expanse 2 inches, grey with dark brown dots and two wavy brown cross bands on the outer third. May and August. Eggs. — Cylindrical, with surface marked with rows of hexagonal depressions; }/3o inch long. Larva. — A geometrid or measuring caterpillar, 2 inches long; green to brownish-black in color, with indistinct green or yellow lines and spots. Full grown in July. PupcB. — Pupae dark brown, ^ inch long, formed in the ground. Some change to moths in August, but others do not change until following May. Lime Tree Winter Moth (Erannis tiUaria Harris).— Occasionally injurious to the leaves of elm, basswood, hickory, apple, etc. Adult. — Male, with rusty-bufif body and fore wings, and lighter hind wings. Female wingless, light brown to grey with markings. Oct.-Nov. Eggs. — Cream colored, cylindrical with ends blunt-rounded. Hibernate. Larva. — A bright-yellow looper, with rust-colored head, and ten crinkled black lines along the back. Full grown larva \Y4.~'^Y2 inches. June. Pupa. — July-Oct. Currant Span Worm {I tamer a rihearia Fitch). Adult. — A pale yellowish geometrid moth with brownish spots, 13^^ inches expanse; markings on wings variable and often with one or two cross bands. Mid-summer. Eggs. — Laid on twigs about July; hatch the following spring when leaves are full grown. Larva. — A yellow striped and black spotted looper, a little more than an inch long; full grown in 3 to 4 weeks. Pupa. — Formed just beneath the surface of ground; duration 2 to 3 weeks. One brood each season. Control. — Spray with arsenical or pyrethrum. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 207 Mottled Umber Moth (Erannis defoliaria Clerck). — Destructive in plum and cherry orchards on the Pacific slope. A European insect, resembling the basswood or lime tree span-worm {Erannis tiliaria) . Adult. — Appears in November; female wingless, brown, with rows of brown spots; fore wings of male dull ochre-brown, crossed by two dark waved bands; hind wings pale and mottled with brown dots. Larva. — Active in June-July; a span-worm, with black stripes sepa- rated by reddish-brown stripes; spiracles in reddish-brown blotches. Bruce's Measuring Worm {Rachela bruceata Hulst). — Destructive in New York in 1886 and in Alberta in 1902-3. Adult. — Female wingless, 3^^ inch long, light brownish-grey; male winged, expanding i}^^ inches, pale brownish. Oct.-Nov. Eggs. — Reddish-orange, oval, finely pitted; laid singly in crevices of bark; hatch in April. Larva. — Three-fourths inch long, apple-green, with three narrow yellowish-white stripes along each side of body; head and thoracic shield black; feeds 4 or 5 weeks in April and May, especially on blossom buds. Pupa. — -Light brown in a slight silk-lined cocoon in the ground. One generation in a season. PsYCHiD^ (Bag-worm Moths) Evergreen Bag Worm {Thyridopteryx ephemermformis Ha worth). — Occurs on conifers, red cedar and arbor vitae. Adult. — Female wingless, naked and grub-like; male with trans- parent wings. September-October. Eggs. — Deposited in a mass within a bag composed of silk mixed with bits of leaf and twig in September-October. They winter over and hatch in May-June. Larva. — Feed on the leaves within bags which are gradually en- larged as they mature. PupcB. — Formed within the bags. Control. — Spray foliage with arsenical solution; gather cocoons and bags. PYRALIDINA GROUP Families (After Comstock) E. Wings not fissured. F. Hind wings without a fringe of hairs at base of Cubitus. 2o8 ECONOMIC ENTOMOLOGY G. Fore wings with fourth and fifth branches of Radius separate, the latter arising from the discal cell. — Pyrauslida. GG. Fore wings with fourth and fifth branches of Radius united at base. — PyralididcE. FF. Hind wings with a fringe of hairs at base of Cubitus. G. Radius of fore wings 5-branched. H. Maxillary palpi more or less developed but not triangular as in HH. — Galleriidce. HH. Maxillary palpi well developed, appearing triangular; labial palpi long, straight and projecting forward. — Crambida. GG. Radius of fore wings 4-branched. — Phycitlda. EE. Wings fissured. F. Wings with less than five fissures. — PterophoridcB. FF. Wings with five fissures. — Orneodidce. Pyralidid^ Meal Snout Moth {Fyralis farinalis Linn.). Adult. — A pyralid moth, I inch wing expanse. Fore wings with base and tips dark brown, middle portion Hght brown, two wavy white Hnes crossing wings, bordering the middle portion, hind wings grey with two wavy whitish lines. Eggs. — ^Laid in masses; irregular. Larva. — ^Lives within a silken tube; dirty-grey, darker at both ends; head brownish-red. Pupa. — Brownish-red, in a cocoon. Clover Hay Worm (Hypsopygia costalis Fab.). — The caterpillars cause injury to stacked or stored clover, near the ground or floor, by webbing it together and contaminating it with excrement. AduU.~^ma\\; ^i inch wing expanse; wings silky, margined with orange and fringed with golden yellow; two large golden spots at the thirds of the fore wings, extending to hind margin as narrow lilac lines. Two straw colored lines on hind wing. Under surface of wings pale yellowish; head and legs straw colored; antennae and palpi pale orange. Two broods. June-July; August. Eggs. — ^Laid probably on growing clover heads. June and August. Larva. — Three-fourth inch long, dull brown; head, shield and anal plate black after last moult; segments much wrinkled and provided with several smooth shining areas each bearing a fine white hair. Hibernates. Pupa. — Honey-yellow; cocoon }2 inch long, oblong-oval, white, silky, intermingled with excrement and bits of hay. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 209 Control. — Remove old hay and if infested burn it; raise stack above ground a few feet on old rails, etc. Salt bottom of stack. Grape Leaf Folder (Desmia funeralis Hhn.). — Occurs on wild and cultivated grapes, and is widely distributed over the United States and Canada. Causes injury by skeletonizing the upper surface of leaves, while protected under their folds. Adult. — Wings expanded, %o inch, dark brown and bordered with white. Fore wings with two oval white spots; hind wings of male with one spot, of female spot divided. Body black, crossed by two white bands in female, one in male. Antennae of male knotted near the middle. Two broods; May and July-August. Eggs. — Minute, elliptical; laid singly on under side of leaf. Dura- tion 8-10 days. Larva. — One inch long when full grown; widest in middle; yellowish- green on sides; head and prothoracic shield light brown; sides of first two thoracic segments with light brown spots; six instars. Duration about 4 weeks. First brood matures in July, second in Sept.-October. Pupa. — Formed usually on the ground among fallen leaves. Dark brown; tapering posteriorly. Hibernates. Parasites. — Apanteles, Meteor us, Mesochorus, Exorista, Tachino- phyto and others. Control. — Spray with arsenate of lead shortly after blossoms have fallen. Purple-backed Cabbage Worm {Evergestis rimosalis Guen.). — Injuri- ous in the Maritime Provinces and Southern States to turnips and cabbages. Adult. — Small, wing-expanse % inch; fore wings pale satiny- yellow with a heart-shaped discal spot, two transverse wavy lines across middle of wings, a less distinct line near base and another near tip; hind wings silvery- white with a clear black margin. June and Oct.-Nov. Eggs. — Bright yellow; laid in masses of 20-40 on under surface of leaf; hatch in a week. Larva. — Three-fourth inch long; bristly, slender, tapering to each end; back purplish; head, anal plate and two spots on second segment black. July and Sept. -Oct. Full grown in 2 to 3 weeks. Pupa. — Winters as a chrysalis. Two broods in a season, the last brood being the more injurious. Probably three broods in the South. 2IO ECONOMIC ENTOMOLOGY Control. — Same as for imported cabbage worm (Pieris rapes), p. 176. Sugar Beet Web Worm (Loxostege sticticalis Linn.)- — Injurious in Manitoba, Saskatchewan and Alberta to alfalfa, turnips, rape, onions, peas, cabbage, and other garden plants; in the middle western states and the prairie provinces on sugar beets. A native of Europe and Northern Asia. Adult. — A purplish-brown moth, with darker and paler bands; wing expanse i inch. May and June. Eggs. — Broadly oval, 3^^5 inch long, pale green; laid in clusters (3-10) on the leaves. Larva. — One inch long, dark with a white stripe down the back and one on each side, marked with many black and white tubercles. In Colorado the first brood of larvae feed on pigweed and alfalfa in June; the second brood appears in July, and sometimes injures beets; the third brood about middle of August is most injurious. Most of the larvae hibernate in the ground m long silken tubes. Pupa. — The pupa is formed in early spring in the silken tube. Greenhouse Leaf Tyer {PhlyctcBnia Jerrugalis Hbn.). — A serious pest in greenhouses to violet, rose, carnation, and other plants; and outdoors to beet, celery, lettuce, sweet pea and other plants. It ties up con- tiguous leaves by webs and feeds within, skeletonizing the leaves. Widely distributed. Adult. — A small moth, ^ inch wing expanse; fore wings light brown and with blackish cross lines; hind wings grey with darker margins. Eggs. — Translucent, oval disks, 3^^2 inch long; laid in clusters of 8 to 12; hatch in 19-20 days. Larva. — Three-fourths inch when full grown; greenish white with a green line down the back and another on either side; head straw colored; mottled. Full grown in 3-5 weeks; feeds mostly at night. Pupa. — Formed within the webbed leaves. Control. — Spray or dip the plants in solution of arsenate of lead as soon as larvae are observed; hand pick infested leaves. Crambid^ (Close-wings) Root or Sod Web Worms {Cr ambus spp.).^ — In July and August many small greyish moths with closely folded wings and with project- CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 211 ing mouth-parts (labial palpi) are common on grass lands and collect in large numbers about lights. The caterpillars of these moths live in the sod in silk-lined burrows among the roots of the grass, feeding upon them. Corn is sometimes injured. Adults. — Several species; yellowish- white wings with silver stripes, bands, gold lines and other markings. Two broods. June-July. Eggs. — ^Laid in grass land in June- July and again Sept.-Oct.; oval, yellowish, ridged, 200 by each female; hatch in 6-10 days. LarvcB. — Color varying from yellowish- white to pink to reddish; surface tubercled with tufts of bristly hairs; form loose silken webs and feed on the roots; full grown in 5 to 7 weeks; 3^^ to ^ inch long. Hibernate in webs partly grown. PupcB. — Cocoons formed often in the larval webs; 12 to 15 days. Control. — Plow land early in autumn to prevent egg deposition; plow early in spring; use trap-lanterns to catch the moths. Cranberry Girdler {Cramhus hortuellus Hbn.). — (See Bull. 554, Bur. Ent. U. S. Dep. Agr.) An injurious pest of cranberry vines, widely distributed in United States and Canada. Its host plants are certain grasses, Scirpus americanus, and cranberry. The moths appear in June, and eggs are laid on the trash covering the ground. These hatch in about 10 days. The larva feeds through- out the summer and fall; when full grown it is about half an inch long, with dark brown or black head, light amber colored thoracic shield and tip of abdomen, and sooty-white body bearing many long and short hairs black at the base. It forms cocoons in October-November, but pupates following spring. Duration of pupal stage about 3 weeks. The cocoon is composed of scraps of ground debris — bits of dead leaves, bark, twigs, fine roots, grasses and sand — held together by strands of silk. Its interior is lined with silk. Variable in shape, but usually enlarged at one end. Control. — Fall flooding after picking the crop; sanding; pruning. Larger Com Stalk Borer {Diatraa saccharalis Fab.). — A serious pest of Southern corn fields, originally of sugar cane. The caterpillar feeds early in the season on the "throat" of the young corn, destroying the growing tip, and later feeds as a borer in the lower stalk, where it hibernates. Adult. — A pale brownish-yellow moth, wing expanse of i}'i inches, fore wings darker than hind wings and bear faint markings. Wings 212 ECONOMIC ENTOMOLOGY held close to body when at rest. First brood appears April ist to May 15th; and second brood May 15th to July ist. Eggs. — Flat, scale-like, circular, ^{qq inch long, placed in rows overlapping one another (2-25) on under side of a lower leaf; creamy white at first; hatch in 7 to 10 days. Larva. — Robust, dirty-white caterpillar i inch long, thickly covered with roundish dark spots each with a single bristle; head and thoracic shield brownish-yellow. Hibernating larva is unspotted. Summer duration 20 to 30 days. Pupa. — ^Light yellow changing to rich mahogany-brown, % inch long. Pupation in the stalk; duration 7 to 10 days. (Consult Farmers' Bulletin 634, U. S. Dept. of Agr.) Pyraustid^ European Com Borer (Pyrausia nuhilalis Hbn.). — (Consult Bull. 178, Mass. Ag. Exp. St.) A pale yellowish or reddish brown moth of about I inch wing expanse, introduced from Europe into Massachusetts, whose larva bores into corn stalks. Its wild food plants are barnyard grass, foxtail, pigweed, and its cultivated food plants are corn, hemp, hops and millet. A possible serious enemy of corn. Galleriid^ Bee-moth {Galleria mellonella Linn.). — Known also as Wax-worm. Often a serious pest of bee-hives feeding on stored combs and honey, and combs occupied by bees. Adult. — Wings ashy-grey, hind part of fore wing bronze colored; body brown, about ^g inch long. Appears April 15th to May 15th, and again in July; lays her eggs in hives in crevices at night. Eggs. — Elliptical, 3-^0 inch long, pearly white — hatch in 12 days. Larva. — ^White; i inch long; feeds at night, and makes silk-lined tunnels in the comb. Pupa. — Formed in a tough cocoon on side of hive. Hibernates. Life-history. — In the north two broods appear — the first in May, the second in July-August, and under favorable conditions it requires only 6 weeks from egg to adult. Control. — Keep colonies strong; keep Italian bees; use well made hives, fumigate with carbon bisulphide. classification and description of common insects 213 Phycitid^ Apple Leaf Crumpler {Mineola indigenella Zeller).— A widely distributed moth but injurious mainly in the Central States on buds in early spring. Adtilt. — Wing expanse ^^ inch; fore wings brown with patches and streaks of silver. Emerges in June. Eggs. — Laid in midsummer and hatch in about a week. Larva.- — Three-fifth inch long when full grown; greenish brown, head and thoracic shield dark brown; young larva brown, feeding on leaves of tender shoots; construct crooked cornucopia-like cases of fras and silk. Winters as half grown larva. Injures the buds in spring. Full grown in June. Pupa. — Reddish-brown. Control. — Early spraying with arsenate of lead. Apple Leaf Skeletonizer {Psorosina hammondi Riley). — Sometimes injurious in Mississippi Valley especially on nursery stock, but not common northward and eastward. Adult. — A pyralid moth, }/i mch wmg expanse; fore wings glossy, purplish-brown, marked with two transverse silvery grey bands. Two broods a season. May-June and August. Larva. — Small, Y2 iiich long, greenish or brownish, with 4 black shining tubercles on back behind the head, and with a broad darker stripe along each side of back. Feeding singly, or in groups, in July and Sept.-Oct., on upper surface of leaves under a silken web, skeleton- izmg them and giving them a rusty blighted appearance. Pupa. — Formed among the leaves in a slight cocoon; pale brown, }y'i inch long. Mediterranean Flour -moth {Ephestia kuehniella Zeller) . A dull.- — A pyralid moth, Ig inch wing expanse. Fore wings grey with transverse black zigzag lines; hind wings greyish white with a darker border. Both wings fringed. New generation every two months; lives about a week (Fig. 133). Eggs. — White, elongate oval; a female depositing as many as 200 eggs singly in flour, in cracks, and about machinery; hatch in about a week. Larva. — Cue-half inch long; white with fine black dots, sparsely cov- ered with hairs. Feeds within a silken tube and spins a silken web, 214 ECONOMIC ENTOMOLOGY matting the flour together and causing much damage. Full grown in 40 days. Pupa. — Formed in a cocoon; duration 11 days; cylindrical, reddish- brown above and lighter below; a cluster of small hooklets at tip of abdomen. Control. — Fumigate with carbon bisulphide, carbon tetrachloride or hydrocyanic acid gas; or better still raise room to high temperature of 120-130° for 6 hours. Fig. 133. — Mediterranean flour moth (Ephestia kuehniella) : a, moth; b, same from side, resting; c, larva; d, pupa; e, abdominal segments of larva; a-d, enlarged; e, more enlarged. {After Chittenden, U. S. Bur. Ent.) Indian Meal -moth (Plodia inter punctella Hbn.). Adult. — A pyralid moth, ^ inch wing expanse. Fore wings with outer portion red- dish-brown with fine transverse markings, the middle copper and the inner portion grey; hind wings grey. A new generation in about five weeks. Eggs. — Small, whitish; as many as 350 eggs laid either singly or in clusters; hatch in 4 days. Larva. — One-half inch long, whitish or pinkish, sparsely hairy. Pupa. — Cocoon elliptical-cylindrical. Gelechiid.^ Angoumois Grain Moth {Sitotroga cereal ella Oliv.). Adult.— A small moth like a clothes moth; % inch long; yellowish-grey. Hind wing dark grey, bordered with fine silvery fringe. Fore wing with a black dot between base and middle. Eggs. — Milky-white to pale red;3^^o i^ch long; bottle-shaped; 60-90 eggs hatching in 4 to 10 days. J CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 215 Larva. — Body white, densely covered with bristles, tapering slightly backward; head and antennae brown. Feeds within the kernel of grain. Pupa. — One-fifth inch long, brownish, ovate; eyes black. Formed within kernel. Peach Twig Borer {Anarsia lineatella Zeller). — Destructive to grape roots, peach and other trees in California and British Columbia and troublesome also in the East. Adult. — Dark grey; wings fringed with yellowish-grey, fore wing marked with blackish-brown spots or streaks; expands 3^^ inch; several broods each season. Eggs. — Yellowish-white, elongate-oval; laid on bark of new twigs near base of leaves; duration about 10 days. Larva. — One-half inch long; dull reddish-brown with dark-brown head; winters in silken cases beneath outer bark at base of new growth; first brood attacks young growth, second brood attacks tips and fruit, third brood the fruit. Pupa. — Reddish-brown, }/i inch long; duration 10-12 days. . Control. — ^Lime-sulphur just after buds begin to swell. Palmer Worm {Dichomeris ligulella Hiibner). — (Consult Bull. 187, Cornell Agr. Exp. Stn.) Adult. — A minute brownish-grey tineid moth, expanding % inch; fore wing sprinkled with black scales, and marked near middle with 4 black marks; hind wing fringed, dusky. July. Hibernates as adult. Eggs. — Probably laid in May, and hatch in 2 weeks. Larva. — Skeletonizes the leaf and eats holes in the young fruit of apple; a small caterpillar, \'2 inch long; brownish-green; head light brown. Dorsal surface with two lateral and two dorsal whitish stripes. June. Pupa. — A small brown object attached to leaf by a few silk threads, duration 10 days. The Lesser Bud Moth (Recurvaria nanella Hbn.) , a native of Europe, occurs in the eastern half of the United States and in Nova Scotia, and attacks the buds of apple trees. (EcOPHORIDiE Parsnip Web Worm (Depressaria heracliana DeG.). — A European pest introduced about 1873, feeding on wild carrot and on wild and cultivated parsnips. 2l6 ECONOMIC ENTOMOLOGY Adult. — Greyish buff or pale ochreous, marked with fuscous spots; ^ inch wing expanse; July- August. Eggs. — Laid in May on leaves, stem and on sheath of inflorescence. Larva. — Pale yellow or bluish grey, marked with black tubercles bearing bristles; head and thoracic plate bluish black; 3^^ inch long. Larvae first web the flower-heads together and feed on the flowers and unripe seeds; they then enter the hollow stems and feed on the soft pith. Pupa. — Formed within the hollow stem in a silken cocoon. Dura- tion 2-3 weeks. Control. — Spray carefully the flower-heads as soon as webbing is observed with an arsenical, j iEcERiiD^ = Sesiid^e (Clear Wings) Peach Tree Borer {Synanthedon exitiosa Say). — (Consult Cir. 54, Div. of Ent., U. S. Dep. Ag.; Bull. 170, Cornell Ag. Exp. St.) A native insect occurring wherever peaches are grown east of the Rockies. Adult. — A slender dark-blue clear-winged wasp-like moth. Male moth with wings transparent and bordered with steel blue; expands I inch. Female moth with fore wings blue and clothed with scales; hind wings transparent resembling the male; a broad orange band about middle of abdomen; expands 1)2 inches. July-September. Eggs. — Minute, oval, yellowish-brown; and hexagonally sculp- tured; truncate at one end; deposited on the bark near surface of ground. Each female may lay from 300-400 eggs; hatch in about 10 days. Larva. — One inch long when full grown, robust, yellowish-white, with head and first segment white. Young larva bores into sap- wood at or below surface of ground, and continues feeding well into the fall, and after hibernating resumes feeding in spring, reaching full growth from July ist-September. Exudation of gum mixed with bits of bark and excrement. Pupa. — Cocoon-like cell elongated, made of grass and bits of bark attached with gum and threads of silk. Duration about 3 weeks. One generation each year. Control. — Probe or cut out the caterpillar in fall or early spring; mounding up the earth about base of tree in spring; protect trunk with paper or wire covering or netting (see Ohio Bull. 329). CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 217 Lesser Peach Borer {Synanthedon pictipes G. and R.)- — This native insect occurs in most of the Northern States, in Ontario, and in some of the Southern States, and frequently does considerable injury. The larva bores as a rule above the soil level on the trunks and branches. Winter is passed as a larva, the pupa is formed in the canker or wound, and the moth emerges in June and July. About a month earlier than S. exitiosa. Attack by this insect usually follows mechanical and canker injuries. Imported Currant Borer {Synanthedon tipuliformis Linn.) . A didt. — A small clear- winged moth, ^i inch expanse; body black with a yellow band about the neck, and three yellow bands across the tufted abdomen; fore wings with a margin of blackish scales and a band about one-third from the tip. June. Eggs. — Small, brown, globular; placed in axils of leaves, or in cracks of the canes. Larva. — Bores into pith of cane and makes a long black tunnel in it; when full grown 3^^ inch long, yellowish; head brown; numerous tubercles on body. Half grown by winter; hibernates at bottom of burrow; full grown in May. Pupa. — Pupates in tunnel. Adult emerges in June. Control. — Cutting out and burning the old and afifected canes in fall or early spring. Maple Sesian {Synanthedon acerni Clem.). — A serious borer in soft and hard maple shade trees. Adidt. — A beautiful wasp-like moth, with transparent wings; body slender, yellow, banded trimmed with red, abdomen tufted. May-June. Eggs. — Laid in rough places on trunk. Larva. — A white caterpillar, V2 inch long; head yellow; thoracic shield light yellow. Burrows mainly just below the bark, often in develop- ing tissue. Pupa. — Formed at surface. Control. — Apply soap-carbolic wash early in spring. Squash-vine Borer {Meliitia satyriniformis Hbn.). Adult. — A clear- winged moth, 13^^ inch wing expanse. Fore wings opaque, dark metallic olive-green. Hind wings transparent, veins and fringe black. Abdo- men with orange or black and bronze marks; legs orange; tarsi black with white bands. June- July. 2l8 ECONOMIC ENTOMOLOGY Eggs. — Oval, dull-red; ^^5 inch long; laid singly on stems of plant; hatch in 1-2 weeks. Larva. — Whitish, stout, i inch long; matures in 4 weeks; tunnels in the main stem. Hibernates in the north in a cocoon in the ground. Pupa. — Formed in tough silken cocoons in ground, in spring in North; pupa dark brown with a horn on head and hook-like spines on abdomen; % inch long. Blackberry Crown Borer {Bemhecia marginata Harris).— Occurs from Canada to New Mexico. Adult. — A clear-winged moth, ij^ inches wing expanse; fore wings with a transverse band on outer third; abdomen black, with four bright yellow cross bands; last segment of female yellow, of male black mixed with yellow. Aug.-Sept. Eggs. — Oval, reddish-brown, He inch long; laid singly on under side of leaves, about 140 by each female. Larva. — At first white with a brownish head, hibernating under bits of bark or just below surface of ground. In spring bores into root girdling it; hibernating again in its burrow; in second spring bores upward, and becomes full grown in July. Pupa. — Reddish brown, ^ inch long, 25-30 days; formed in burrow near surface of cane. Empty pupal skin usually protrudes from open- ing when moth emerges. Control. — Remove infested canes during spring and fall when thinning and pruning, and burn them. ToRTRiciNA Group Eucosmidae Apple Leaf Sewer {Ancylis nubeculana Clemens). — (Consult N. Y. State Mus. Bull. 124; Bull. 435, U. S. Dept. of Agr.) Generally distributed over the Northern States and Canada. Adult. — A small white tortricid moth with brown markings; wing expanse ^ inch. May- June. Eggs. — ^Laid in June on under side of leaf; flat, oval-shaped, flanged, minute, yellow; hatch in 8 days. Larva. — One-half inch long; yellowish-green; head yellow; thoracic shield darker with a black dot on each side; each body segment with pale tubercles bearing a single hair. Hibernates in folded leaves on CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 219 the ground. Full grown in April. Total feeding period 5-6 months. Spends the first 3 or 4 weeks of its life under a silken covering on the under side of the leaf, afterward within a succession of folded leaves. It folds the leaf along the mid-rib and forms its nest within. Pupa. — Dark yellowish-brown, but head, eyes and wing shields black mottled with yellow. Duration about 10 days. Pig. 134. — Codling moth. A, adult moth with wings expanded; B, egg much enlarged; C, half of worm-eaten apple; D, cocoon with empty pupa shell protruding; E, cocoon with pupa enclosed; F, leaf and apple showing eggs of a codling moth; G, caterpillar or "apple worm" enlarged; H, a, young apple just after petals fall; b, cup beginning to close; c, too late to spray. {Montana Ag. Exp. St.) Codling Moth {Carpocapsa pomonella Linn.). — This European insect is probably the most destructive of apple insects and is practically cosmopolitan (Fig. 134). Adult. — A small greyish-brown moth, ^ inch expanse; fore wings crossed by alternate irregular transverse waxy bands of brown and grey, and with a large dark brown spot in the inner hind angle; hind wings 220 ECONOMIC ENTOMOLOGY light silky brownish-yellow, darker toward the fringed margin. Flies at night, about 1-2 weeks after the petals fall. Sometimes emerges as late as July ist in northern districts. Eggs. — A minute tliin scale-like white object, I25 inch in diameter, at first transparent but later with a blackish streak. Each female deposits 60 to 75 eggs, mainly on the leaves i to 3 weeks after the blossoms fall; hatch in 5-10 days, or from 3 to 4 weeks after petals fall; 60 to 80 per cent, of larvae enter the young fruit at the calyx end. Larva. — At first whitish with distinct black tubercles on the body and black head ; later the tubercles less distinct. When full grown larva Fig. 135. — Larvse and ptipae of the codling moth in the bark. is f 4 inch long, whitish or pinkish, head dark brown, tubercles indistinct, thoracic and anal shields light brown. Matures in 3-4 weeks. Winters as a larva within a white, tough, silken cocoon (Figs. 134 and 135). Pupa. — Pale brown; ^2 inch long, back armed with transverse rows of minute spines; within a cocoon; duration of spring pupae about 21 days, of summer pups about 15 days (July 3oth-August 14th in Maine). Life-history. — Winters as a full grown lar^•a within a cocoon on the trunk, under bark, etc.; about the time of apple blossoming the larva transforms to a pupa, and the moth emerges 15 to 22 days later. The eggs are laid singly on the leaves, stems, and even fruit, where they hatch in 7 to 10 days. The young larva feeds for a short time on the leaves, but finds its way to the fruit which it enters usually at the calyx end. It then makes its way to the core. When full grown in 3 to 4 CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 2 21 weeks it makes its way out of the apple by a round hole and finds a place under bark, etc., to make its cocoon. WTien a second brood occurs ^PRIL 1 MAT ! JUNE J JULY, [ AUGUST J St I ft W-.l""!--^ i- f T 1 fl-^ -] C^^C^^^^^T^^?^ ^' Over-Winter coei'onsfSee 'bLaJt Fig. 136. — Chart showing life-history of the codling moth with suggested times of spraying and banding in Utah. {After Hagon.) Pig. 137. — The proper time to spray for the codling moth. the moths emerge throughout August, and the second brood larvae enter the apples chiefly from the side. In Northern New England and ECONOMIC ENTOMOLOGY ,r 1 1 o ., >, O o c g o o •d 1 *^ •d MO C Ol « •^ 0. O 3 < So 5s M So C o 0) 1- 1«" " o o, <-• c V T3 0.0. M M M til S U o .S-- » U3°0 tS (U 1) rt O M^ WM« Kmo M " p^a, w O O t-, 1 4^ a! 0) bo >-• g 0) s ^1 3o 1 ■d o 1 fOO M M 3 3 1 M M •« ss 6S 'tn 1 M CA 1 a O lO 1/5 . ■'d 3 D^ ^'^ > O 3 O 4J 3 O •s 4^ I "o m M O Jh« M 4-* Jl,^ » 00 M U (UJ- n o 3 < 3 > 1 3'3 ■— ii— 1 3 u -iW ^^ _^ G 1 O to .- "> fO 05 o 2 " >> )Q>' (S >. •^ N rt N Cj rt to rt ^"^ •d -d .-d ^ Q, >. >. M (U o 3 3 « r-,^^ 3^ 3 '^ 2 4 o 0-3- tS to hJ 8 3 Uoo 3^ "5 "3 t. ^'s s CO —icn— ' '"' P) ^—1 ,— ^ ,— ^ 1 N o 0^ ^•d H 01 1 " Ai'" 3 « !? 3 3 3 3 D ''^ — iW^ ■" 5 '— 1-1 '—m ill « 11 >> 3 3m O tH 4) a 3 3m ^°4 c,SV5 3 3-N 00 "^ Si (0 a 3 1—1 ' — i*— 1 ^ 1 —i si" w t^ P) N t~ 1 O it- 1 N 1 o S o 3 S^^l" &§ ^S 1 tX) , 4^s^ 3 3 3 1-1— > 3 3 S^ S4 ^ ^^ 1 ''"^ I '"^ c _o N " >, .1 ^ ^ >• JJifl" t* l^ M « t^Oj H (3 " in tl) "^ N C4 t-" 3 ft S^^ 2^3 S43 s 3 3 >, 4J K 0. (1h x J O o ■4-J c C o a O 2i s 1 4J O C "a 3 o 1 1- 1 E X 1- c 2 ■ 61 c i c C 1 CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 223 ( 3 >_, Sj IN M >-H •d 0\ o> C 00 0. C\ M rf -^ 1^ vT 2 -S C (D a d . ro . v (N -^ (U J3 1 ^ >< 3 ^ 1— I '~- 60 3 1—1 00 1 M 1 00 o> 1 M >•■£ >.o. 4) 13 _>. >, bi 4<^ 3 (U s- 3 3 r^OT 1-1 -^ ^-^ 1 <" 1 i,"<3 !*• M t- >< N w S 1 M >. N nj M " M .g Oi nl •0 "3 2 '^ S 2 3 3 " — » ,.— s In "m" 1 >. 4.n« >. >. 3<| t- N w >. H CD ro •0 "3 ?! >> 3 1—) '-' 1 ■* ^— ^ ck^ 1 f" N (U C 3 ►-1 a 5 .^ " >■ -! , fO a! Hi M r?^ 1 1 1 ^ ^>" c >. >. ^•S d ca n! Gi e n 3 S^ ss S S4 ^-^ -^ 01 M 1 r^ >> fO mm™ _ •^ ea ■d •d a w-g .u-O >> lU-N a c-N »g 300 rt > J3 ! > < D 1 "a 3 Q 2 '0 m C 224 ECONOMIC ENTOMOLOGY Canada, with the exception of Southern Ontario, there is but one brood a year, with a very small percentage transforming to make a partial second generation, but further south there are two or even three broods. Parasites, Etc. — Trichogramma pretiosa, Trombidium on eggs; Pinipla annulipes, Macrocentrus delicatus, Ascogaster carpocapsa, Itoplectis marginatus, Hypostena variabilis and Tachinophyto on larvae; Pig. 138. — Bud moth. I, Adult moth; 2, larva; 3, pupa (dorsal view); 4, pupa (ventral view). {After DuPorie.) some beetles (Tenebroides corticalis) two species of ants, Lasius niger and Solenopsis molesta, woodpeckers and chickadees. (Consult Bull. 142, Cornell Ag. Exp. St.; Bull. 41, 80, 97, 115, 189, 252, n. s., Div. Ent., U. S. Dep. Ag.; Bull. 187, Ont. Dep. Agric.) Control. — Spray with arsenical just after the blossoms fall, and again in 3 weeks; destroy fallen fruit; band trees about July ist; fumigate fruit-houses with sulphur to kill the moth (Fig. 136 and 137). CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 22$ Bud Moth {Tmetocera ocellana D. and S.)- — (Consult Bulls. 50 and 107, Cornell). — The caterpillar of this moth sometimes does serious injury to the unfolding flower and leaf buds of the apple and other orchard trees. Introduced from Europe, and occurs from the Atlantic to the Pacific. Adult. — A small moth with broad yellowish- white bands across ash colored fore wings; % inch expanse; lives 2-3 weeks. Emerges in June and July and deposits eggs (Fig. 138). Eggs. — Flattened, disk-shaped, transparent; laid singly or in clusters on the under surface of the leaves; hatch in 7-10 days. Fig. 139. — Seasonal history of the bud moth in Quebec. Larva. — Full grown larva 3^^ inch long, chestnut brown sparsely clothed with light colored hairs borne on darker tubercles; head, legs and thoracic shield dark brown or black, smooth and shining. Full grown in June. Winters as half-grown larva in small oval silken cases on bark of twig. Emerges in spring when buds are expanding and bores into the bud and feeds for 6-7 weeks, latterly on the leaves tying them together. Pupa. — ^Light brown; i)^^ inches long; two rows of short blunt back- ward pointing spines on back of abdomen; in a thin closely woven silk 15 226 ECONOMIC ENTOMOLOGY cocoon within a tube of tangled leaves. Pupal stage lasts about lo days. Life-history. — Hibernates as a half-grown larva, and matures in June; pupal stage lasts lo days and moth emerges in July to deposit eggs. Young caterpillars feed on epidermis of under side of leaf and on green tissue within a silken tube for protection. Toward the end of September they leave their silken tubes and form oval silken cases on the smaller twigs near the buds, where they hibernate (Fig. 139). Fig. 140. — Pea moth: a, a full grown "worm" or caterpillar (enlarged); b, adult moth with wings expanded (enlarged); c. adult moth with wings closed; d, a group of five peas injured by the caterpillar of the pea moth. Parasites. — Pimpla conquisitor , Bassus earinoides, Trichogramma pretiosa {Pentarthron minutum), Opius sp., Microdus laticinctus. Control. — Spray with arsenate of lead when buds are expanding, when the leaves are expanded, and before and after blossoming. ArgyroploceconsanguinanaWdX'i\im..\s, another bud pest of occasional importance. Pea Moth {Laspeyresia nigricana Steph.). Adult.— K small grey moth % inch long. July (Fig. 140). J CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 227 Eggs. — ^Laid in the growing pod; hatch in about 2 weeks. Larva. — A small whitish slightly hairy caterpillar with pale brown head and thoracic shield; about }2 inch long when full grown, feeding within the pod on the green peas. Pupa. — In a small oval cocoon in the ground near the surface. Life-history. — Early in July the moths emerge from cocoons in the ground, and begin egg-laying; larvae hatch out in about 2 weeks. About the end of July the larvae emerge from the pods and spin small oval cocoons near the surface where they remain all winter. Control. — Sow early varieties; sow very late; deep fall plowing of infested land; spray after blossoming with soap and Paris green and repeat in 10 days. Lesser Apple Worm {Laspeyresla primivora Walsh). — (Consult Bulls. 68, Part V, and 80, Part III, Bureau of Entomology.) The early work of this worm is similar to that of the Codling Worm, only nearer the surface on the flesh just under the skin; the young larvae hatched in August often eat on the surface of the fruit. Two broods in the Northern States, and one in Quebec and northern Ontario. Adult. — Ground color of fore wings brown with pale rusty-red patches, and with grey, yellowish-white and blue oblique hnes; hind wings dusky grey at base, shading to black at apex. Appears in early June about the same time as the Codling Moth, and again in August. Eggs. — Glistening white, minute, flat, oval, and covered with net- work of irregular ridges. Deposited on both sides of leaves, but on upper surface of fruit, stems, etc; hatch in 4-6 days. Larva. — Full-grown larva 3^^-)^ inch long; reddish flesh-colored above, lighter below; head brown; thoracic shield yellowish, transparent; anal plate brownish, with a brownish comet-like structure on the caudal curvature, and with an anal fork; mature in June and July. Many of the second brood larvae enter the fruit on the side. Time in fruit 2-4 weeks; larva in cocoon before pupation 7-8 days. Larvae of second brood winter over. Pupa. — ^Pupation in spring; cocoon densely lined inside with whitish silk; pupa brown, 3^^ inch long; pupation stage about 10 days. Empty pupal case usually attached to cocoon. Control. — As for Codling Moth but spray again in August; destroy hawthorns in vicinity. 2 28 ECONOMIC ENTOMOLOGY Laspeyresia molesta Busck. — A new species found injurious to peach in District of Columbia. Clover Seed Caterpillar {Laspeyresia inter stinctana Clemens). — (Consult Bull. 134, III. Ag. Exp. St.) Injures heads of red clover, white clover and alsike. Adtdt. — A silky dark brown moth, expanding about )^ inch; fore wings with 8 or 9 silvery markings along the front margin, and 2 curved markings on hind margin forming two crescents when wings are closed; hind wings dark brown with pale fringes. Probably three broods each season. May-June ; July ; Aug .-Sept. Eggs. — At first green, later yello wish- white ; shghtly flattened orbicular; hatch in 5 or 6 days; laid on young clover heads, or on young stems and leaflets near the base. Larva. — One-third inch long; dirty- white to orange; head dark brown and polished; thoracic shield yellowish or dark brown with a clear me- dian line; dorsal tubercles arranged in 2 pairs and bearing hairs; body with several pale stiff hairs. Mature in 4 to 5 weeks. Pupa. — Brown, 3^^ inch long. Cocoon oval, white, silken, usually with bits of flower tissue and excrement attached. Spun in a clover head or at surface of ground. Duration 14 to 30 days. Control.— Cnt and store the clover crop early in June; do not allow clover to run for more than 2 years. Grape Berry Moth {Polychrosis viteana Clemens). — (Consult Bull. 223, Cornell and Bull. 293, Ohio). A serious grape pest causing wormy grapes. Adult. — A purplish-brown tortricid moth, 3^ inch expanse; wings leaden-blue with dark spots. Two broods. Eggs. — Minute, whitish and scale-like, laid on stems of flower clusters or later on the green berries; hatch in 4-8 days. Larva — ^Mature caterpillar, % inch long, dark green to purpUsh; head light brown; thoracic shield black; body covered with many faint spots bearing whitish hairs; 3 weeks. Pupa. — Formed in a thin silk cocoon in a piece of leaf; light green- ish-brown. Duration 10-14 days. Life-history.— In June- July the moths appear and lay their eggs in the blossoms and on young grapes. The young larvae feed on the blossoms and young berries, webbing the clusters together. They mature in 3 weeks and pupae are formed in cocoons made from bits CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 2 29 of leaf and lined with silk. Moths emerge in lo to 14 days in early August. The eggs of second generation are laid on the berries, and the larvae feed on the pulp and seeds. Sometimes there is a third generation. Winter is passed in the pupal stage. Cow/ro/.— Spray with arsenate of lead, 4 lb., Bordeaux 2:3 : 50, and 2 lb. dissolved soft soap just after blooming; in August, when the berries are half-grown, or about 7 weeks after the grapes bloom, use 6 lb. arsenate of lead. TcRTRiciD^ (Leaf Rollers) Fruit Tree Leaf Roller {Cacmcia ar gyros pila Walker).— (Consult Bull. 311, Cornell, Bull. 250, Ont. Dep. Ag.) A serious enemy of the apple east of the Rockies. It attacks also pears and plums, and some shade and forest trees. Fig. 141. — Egg-masses of fruit tree leaf roller. FiG. 142. — Fruit tree leaf Natural size. {After Caesar.) roller: a, female; b, male. Naturaljsize. {After Caesar.) Adult. — Front wings mottled with a rusty-brown shade and silvery- white markings; hind wmgs light ashy brown without markings, ^ inch wing expanse. Early July; one brood each year (Fig. 142). Eggs. — Attached to upper side of twigs in small oval, flat, greyish varnish-covered patches, about 100 eggs in each egg-mass, in July. Hatch as buds are opening. Hibernate (Fig. 141). Larvce. — At first are black-headed and green; tie together the young leaves and blossoms with a silk web, later cut large irregular cavities 230 ECONOMIC ENTOMOLOGY out of young fruit. Injured fruit falls or is deformed. The leaves are also badly injured. Full grown in three weeks; about i inch long; light green; head, thoracic shield and legs brown to black. Pupa. — Formed within a rolled leaf, brownish; duration about 10 days. Control. — Spray with lime-sulphur (32°) and lead arsenate (3 lb. to 100 gal. water) about May 15, June i and June 15; use Scalecide (i to 15) just before leaf-buds burst to destroy the eggs. Cherry Tree Tortrix {Caccecia cerasivorana Fitch). — A pest of cultivated and choke cherries. Adult. — A tortricid moth, expanding about an inch; front wings ochreous yellow with irregular brownish spots and many transverse pale blue bands. July-August. Eggs. — ^Laid in flat gluey-covered masses on twigs mainly near the ground; hibernate; hatch in spring. Larvce. — Lemon-yellow, ^^ inch long; colony forms nest enclosed in silk web. Mature in July. PupcB. — Formed within the dirty ugly nest. Duration 10 to 14 days. Pupal skms project from nest. Control. — Cut out and burn the nests before the moths emerge. Oblique Banded Leaf Roller {Caccecia rosaceana Harris) .■ — Injurious to leaves and buds of orchard trees and small fruits; widely distributed. Adult. — A yellowish-brown tortricid moth with three oblique dark bands across the fore wings; bell-shaped with wings folded; hind wings pale yellow. End of June. Eggs.- — ^Laid in flat patches on the bark where they winter. Larvce. — Roll up and fasten together the young leaves within which they feed; ^ inch long; yellowish-green; head and thoracic shield brown- ish-black; two broods, one feeding in May-June, the other in July- August. Pupa. — A dark brown object formed in its silken shelter in folded leaves. Control. — Spray with arsenate of lead in early spring and July. Caccecia scmiferana occurs on apple. The Large Aspen Tortrix {Caccecia conflictana Walk.) occurred in destructive numbers in Manitoba in 19 16— 17 on aspen poplars, although it is usually a rare insect. According to Criddle the adult emerges in July and lays flat masses of eggs on the leaves. The caterpillars eat CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 23 1 holes in the leaves and spin much silk. About the end of July they go into hibernation resuming feeding in the spring and pupating in July. The natural means of control are hymenopterous parasites, birds, and sudden climatic changes in early spring. Lesser Apple Leaf Roller (Peronea minuta Rob.). — Sometimes inju- rious in Eastern nurseries, causing the leaves to become folded and brown; also a pest of cranberry bogs. Adult. — Small, ^^ inch wmg expanse; fore wings of summer brood bright orange colored; of the autumn brood slaty-grey. Two or three brooded. Hibernates. Eggs. — Minute, disk-hke, yellow; laid on unfolding leaves. Larva. — Feeds within a folded leaf for 3 to 4 weeks. Broods work in May, July and September. Pupa. — Small, 3>i inch long, brown; head with a knob-like projection; within a silken web or cocoon. Duration 7 to 10 days. Spruce Bud Worm {Harmologa Jumifcrana Clem.). — (Consult Bull. 210, Maine Ag. Exp. St. and Hewitt's Reports.) A destructive pest of spruces in Northern United States, Eastern Canada, Manitoba and Vancouver. Adult. Fore wings brown, varied with short dark brown striae; hmd wings dark fuscous. July. Eggs. — Pale green, scale-like, flat; laid in patches overlapping each other. Hatch in about 10 days. Larva. — When young pale green with a yellowish tint; head dark brown, thoracic shield amber with two dots on posterior margin; hairs half as long as thickness of body 3^^ i^ich long. Just before last moult uniformly rust-red brown, and head and shield black. Full grown larva with thick stout body tapering from middle to end; head not quite so wide as body, and dark brown. Feeds on needles of terminal shoots, often separating them at base and spinnmg a silk thread about them and the bud scales. Hibernates among the terminal shoots, becoming full grown the following June- July. Pupa. — Thick; thorax swollen; pale brown color striped with brown; antennae and legs dull tan color. Parasites. — Winthemia fumiferance, Pimpla Inquisitor and P. con- quisitor, Meteorus trachynotus, Conoblasta fumiferancB, Mesochorus diversicolor, Epiurus innominatus. 232 ECONOMIC ENTOMOLOGY Strawberry Leaf Rollers {Ancylis comptana Frohl and Caccecia ohsole- tana Walker). — These two tortricids often do injury to strawberry leaves by rolling and destroying them. They may be controlled by spraying the plants with a solution of lead arsenate (5 lb. to 100 gal. water) within a week after the first appearance of the Moths. Heliozelid^ Resplendent Shield Bearer (Coptodisca splendor if erella Clem.). — Sometimes a serious pest in orchards. Found from Maine to Minnesota. Adult. — A small brilliantly colored golden-headed moth; fore wings leaden grey and lustrous at base, outer portion golden with silver and dark brown streaks; hind wings rich grey with long yellowish fringe; antennae brown tinged with gold. May-June. Eggs. — ^Laid on leaves. Larva. — Small, 3^^ inch long, legless, light yellowish brown; head dark; makes an irregular dark blotch mine )^ inch in diameter, in the leaf. When full grown in July it cuts out a portion of the mine and forms a seed-like yellowish shield, which is attached to bark. A second brood in September, and in October the seed-like pupa case is formed. Pupa. — In an oval, disk-shaped seed-like case. Hibernates. Plutellid^ Diamond-back Moth {Plutella maculipennis Curtis). — A widely distributed insect in U. S. and Canada. The caterpillar occasionally attacks the leaves of turnips and cabbages, and does considerable injury. Adult. — A slender moth of a general ashy-grey color with white marks on the back, diamond-shaped when wings are closed; % inch wing expanse. Eggs. — Minute, scale-like, greenish white or yellowish, laid singly on lower surface of leaves. Larva. — ^A minute, active, dull green caterpillar with spindle-shaped body and with a wriggling motion when disturbed; mature form ^0 inch long; feeds on the lower surface of the leaves; effects visible in July. Pupa. — Slender, yellowish, 3^4 inch long, enclosed in a beautiful white lace-like cocoon on the surface of the leaves. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 233 Probably two or more broods in a year in Canada; seven broods at Rocky Ford, Colorado. Control. — Broadcast 2 to 3 cwt. ground lime per acre on appearance of moths on a dewy morning. Brush off caterpillars. Spray the caterpillars with kerosene emulsion, care being taken to get the solution on the under surfaces of the leaves. Yponomeutid^ Apple Fruit Miner (Argyresihia conjugella Zeller). — Occurs in western portions of Canada and the U. S. Adult. — One-half inch spread; fore wings purplish-grey mottled with brown, with a row of small white and brown dots on front margins and a broad white interrupted band. May- June. Larva. — Pinkish-white; % inch long; burrows in all directions through fruit. Also on wild crab. Pupa. — In white cocoon with open pattern, under bark or leaves. White Cedar Twig Borer {Argyresthia thuiella Pack.). — Causes a rusty appearance on white cedars along the Ottawa. Adult. — A small pearly white moth with costal and apical brownish spots; head and thorax white; antennae white with brown rings. Latter half of June. Larva. — Slender, olive green, brownish at anal end; head black and shining; thoracic shield piceous; 3^^ inch long before winter sets in; hibernates in mines made in the young twigs; renews growth at end of May and is 3>'4 inch long when full grown in June. Pupa. — ^No cocoon; formed in the mines. The Apple Ermine Moth (Yponomeuta malina) and the Cherry Ermine Moth (Yponomeuta padella L.) are destructive orchard pests in Europe. They reached the U. S. in 1914 on nursery stock imported from France into New York State, and were discovered in shipments of ornamental shrubs and fruit seedlings into New Brunswick in 191 7. The moths are small, about f-^ inch wing expanse; fore wings white with black dots; hind wings grey and broadly fringed. The caterpillars are about % inch long and vary in color from pale to greyish or greenish brown. The moths fly during July and August; the eggs hatch in the fall and the young larvae hibernate beneath the scaly covering formed by the egg-masses. 234 economic entomology Haploptiliid^ Case Bearers. — Two species of Case Bearers are found in apple orchards: the Cigar Case Bearer, and the Pistol Case Bearer. They do most injury to the young buds and blossoms. I. Cigar Case Bearer {Haploptilia fletcherella Fernald).- — (Consult Bull. Q3, Cornell Ag. Exp. St.; Bull. 80, Ft. II, Bur. Ent, U. S. Dep. Fig. 143. — a. Cigar case bearers and their work on apple leaves; b, pistol case bearer and its work on young fruit. Natural size. {After Caesar.) Ag.) Adult. — A small greyish moth, expanding 1^ inch; wings broadly fringed. June-July (Fig. 143, a). Eggs. — Delicate light lemon-yellow; pitted; cylindrical; laid singly on under sides of leaves; hatch in 10-14 days, about July 15th. Larvce. — Orange colored; head black; feed as miners for 2-3 weeks within the leaf, then later in curved cases on the leaves. About CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 235 September 15th they migrate to the twigs where they hibernate in their cases. About April 15th they attack the young buds, etc.; about the end of May they make their characteristic cigar-shaped cases, within which they feed on the leaves. About the end of June they change to pupae. Pupa. — -Light brown; duration about 10 days. 2. Pistol Case Bearer {Haploptilia malivorella Riley) .^ — (Consult Bull. 124, Cornell Agric. Exp. St.) The life history of this species is very similar to that of the Cigar Case Bearer, the habits of the larvae differing to a slight extent (Fig. 143 h). Adult. — A minute moth with brownish, heavily fringed wings and covered with white scales, head and thorax white; abdomen whitish; all parts dotted with brown scales. June- July. Eggs. — -Cinnamon-rufous; like inverted tea-cups with strongly ridged sides; July; egg stage lasts about a week. LarvcB. — Never miners; make cases as soon as they begin to eat. In September they migrate to twigs where they pass the winter in small pistol-shaped cases. In spring they attack the buds and make irregular holes in the leaves. About the beginning of June they change to pupae. Pupa. — Pupal stage lasts about 2 weeks. Control. — Spray with arsenate of lead in early spring just before the blossoms open and in July. TiscHERiiD^ (Leaf Miners) Apple Leaf Miner {Tischeria malifoliella Clemens). — The larva forms trumpet- shaped blotches under the surface of the leaves. Adult. — A minute moth expanding }i inch; wings broadly fringed. Fore wings shining dark brown with a purplish tinge; hind wings grey; head and antennae dark brown. May. Eggs. — Small, greenish-yellow, blister-like, elliptical, }yio inch long; attached to surface of leaf. Hatch in 8-10 days. Larva. — A miner within the leaf; mature in 3 weeks. Larvae of last generation hibernate in the fallen leaf. Pupa. — Pupa formed within the leaf. Duration 8-10 days. Two or three generations each season. 236 economic entomology Lyonetiid^ (Leaf Skeletonizers) Apple Leaf Bucculatrix {Bucculatrix pomifoliella Clemens). — (Consult Bull. 214, Cornell.) Adult. — A small moth, }^ inch expanse; fore wings whitish tinged with pale yellow and dusky brown. Hind wings broadly fringed. Appears when leaves unfold. Eggs. — ^Laid in May, singly on under side of apple leaves; elliptical, Mo X H25 inch, greenish, iridescent; surface rough. Larva. — One-half inch long, cylindrical, tapering at both ends; dark greenish-yellow, with reddish tinge on anterior segments, active. Full grown in July. Pupa. — Cocoons dirty white, slender, }^ inch long; six prominent longitudinal ridges; oblong, tapering at both ends; fastened to twigs in groups, in September-October, etc. Hibernates in this stage. Birch Leaf Skeletonizer (Bucculatrix canadensisella Chamb.). — A serious pest of birches, skeletonizing the leaves. Adult. — A small brown moth, about M inch long; wings crossed with fine white bars. Larva. — Slender, green; head brown; tapering slightly toward both ends. It spins a small round white moulting cocoon on the twigs or leaf, and later spins a yellowish ribbed elongate cocoon within which it pupates. Control. — By parasites and by spraying with arsenical solution. TiNEiD^ (Tineids) Clothes Moths. — Three injurious species of Clothes Moths are rec- ognized in America: (i) Case-making Clothes Moth, (2) Webbing or Southern Clothes Moth, and (3) Tapestry Moth. I. Case-making Clothes Moth {Tinea pellionella L.). — So-called because the larva makes a true transportable case. (Consult Circ. 36, Bur. Ent., U. S. Dept. Agr.) Adult. — A small tineid moth expanding 3^^ inch; head and fore wings greyish yellow; hind wings greyish white and silky. June-August. Eggs. — Minute whitish, placed directly on foocj material; hatch in about 10 days. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 237 Larva. — A dull white caterpillar with head and upper part of neck segment brown; living within its case; feeds on woolens, carpets, furs, feathers, etc. Pupa. — Formed within larval case; duration about 3 weeks. One generation a year in the North. 2. Webbing or Southern Clothes Moth {Tineola biselliella Hum.). — Two or more broods in the North; more common than the preceding in the North. Adult. — Fore wings pale ochreous. Female larger than the male; lays 4c^5o eggs. Eggs. — ^Laid among the threads of the cloth; hatch in 7 days. Larva. — Constructs no case, but spins a silky cobwebby path wherever it goes; full grown in 10 or more weeks. Feeding all months of the year on woolens and furs. Not readily poisoned. Pupa. — Cocoon stage 2 or more weeks. 3. Tapestry Moth (Trichophaga tapetzella L.). — Rarer and slightly larger than either of the preceding. Adult. — Head white, basal half of fore wings black; outer half creamy and grey; hind wings pale grey. Expanse ^^4 inch. Larva. — Burrows in food materials, lining them with silk — no other protection than the galleries or burrows it makes. Feeds on carpets, horse blankets, tapestries,, felting, furs, skins and woolen upholstering of carriages. Control. — Give clothes or carpets a thorough beating, spray with benzine and expose to sun for some hours, and repeat frequently. C0SSID.E (Carpenter Moths) Leopard Moth (Zeuzera pyrina Linn.). — A serious pest of shade trees in the East, especially of elm and maple. A native of the old world. Adult. — A white moth with blue and black markings; female much larger than male and a feeble flyer. Male with pectinate antennae; wings semi-transparent and white with black markings; thorax with six large and one small black spot. Eggs. — Oval, salmon-colored, deposited either singly or in a large mass in crevices of bark; hatch in about 10 days. Larva. — White or pinkish, over 2 inches long when full grown; numerous dark tubercles with hairs on body; head, thoracic and anal shields brown. Bores along the pith, eating the wood at intervals, 238 ECONOMIC ENTOMOLOGY with an occasional opening for the removal of fras, which is soon closed with a web of silk. Both large and small hmbs when attacked fre- quently break off. Nearly full grown by second winter. Pupa. — Formed in the burrow in May of second year. Control.- — Prune away and burn the smaller injured twigs or branches; inject carbon bisulphide into the openings of burrows and seal with wax or putty. Carpenter or Goat Moth {Prionoxystus robinicB Peck.).— The cater- pillar bores into maple, oak, ash, willow and locust trees, often producing deformities. Adult. — A large moth, wing expanse of female 3 inches, of male 2 inches. Color dark grey mottled with light grey. Front wings of male darker, and hind wings ochre yellow. June and July. Eggs. — Oval, 3^fo inch long; each female lays several hundred eggs; dirty whitish with one end black; finely reticulated, sticky. Laid in crevices about injuries. About July ist. Larva. — A large white caterpillar suffused with rose red, 2)^^ inches long; head brownish, jaws prominent and black; thoracic shield dark brown in front; each segment with several minute brownish tubercles, each bearing a hair; spiracles brownish; a dark-colored dorsal hne; under side of larva greenish white; bad smelling. Pupa. — Brownish, i)^ inches long; dorsal surface of abdominal segments with rows of tooth-hke processes. Formed in a loose cocoon at ends of galleries. Duration 2 weeks or longer. The life-cycle is believed to occupy 3 years. Control. — Trim away deformities; inject CS2 into borings and close holes with putty or cement. Nepticulid^ Serpentine Leaf Miner {Nepticula pomivorella Pack.). Adult. — A minute, purpHsh-black tineid moth; head tufted; reddish-yellow; June. Larva. — Small, dark-green caterpillars Ho inch long. Make a narrow serpentine mine beneath surface of leaves of apple and pear, first half of mine broader than second half. In late autumn the larvae find their way to twigs by means of silken threads, where they spin small oval brown cocoons % inch long resembUng Lecanium scales. In May they transform to pupae. Pupa. — Bright green. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 239 ORDER DIPTERA (FLIES) Sub-orders and Groups A. Adults without a frontal lunule; pupa and adult escape from larval skin through a T-shaped opening at anterior end. — Sub-order Orthorrhapha. B. Antennae long, with more than five joints. — Nematocera Group (Fig. 144, A). BB. Antennae short, usually 3-jointed; first anal cell narrowed. — Brachycera Group. (Fig. 144) A A. Adults with a frontal lunule; pupa and adult escape from larval skin through a circular opening at anterior end. — Sub-order Cyclorrhapha. Fig. 144. — Antennae of common Diplera. A, Xiphuria (Tipulidse). B, Sargus (Stratiomyiidas). C. Stratiomyia (Stratiomyiidas). D, Culex (Culicidas). E. Tabanus (Tabanidae). F, Leptis (Leptidag). G, Chrysops (Tabanidge). H, Anthrax (Bombyliidse). /, Dasyllis (Asilidae). J, Bibio (Bibionidae). K, Gonia (Tach- inidse). L, Pollenia (Muscidae). Chief Families of the Nematocerous Orthorrhapha: A. A distinct V-shaped suture on back of thorax; legs long and slender. — TipulidcB (Crane Flies) p. 242. AA. No V-shaped suture on thorax. B. Veins and margin of wings fringed with scales. — CulicidcE (Mos- quitoes), p. 243. BB. Margin of wings not fringed with scales. C. Anal veins wanting; Media vein wanting; tibiae without spurs. — CecidomyiidcB (Gall Gnats), p. 245. CC. Anal veins present and Media vein at least represented by a fold. Costal vein does not extend beyond tip of wing. 240 ECONOMIC ENTOMOLOGY D. Abdomen slender; wings narrow; antennae pulmose in the males; wing veins strong near costal margin. — Chiro- nomidce (Midges), p. 252. DD. Abdomen short and thick; wings broad; antennae short and non-plumose. — Siniuliida (Black Flies), p. 251. Chief Families of the Brachycerous Orthorrhapha (Figs. 146-149); A. Antennae of five or more segments, those beyond the second more or less united. (Fig. 144, E). Fig. 145. — Venation of a tipulid {Tipida). (After Comstock.) Pig. 146. — Venation of a tabanid {Tabanus). {After Comstock.) AA. B. Alulets large, third joint of antennae without a style or bristle. — Tabanidce (Horse Flies), p. 252. BB. Alulets small; branches of Radius crowded together near the costal margin.- — Straliomyiidce (Soldier Flies). Antennae of four or five segments but the third joint not ringed. B. Antennae long, clavate, 4- jointed; branches of Radius curving toward costal margin. — Midaidce (Midas Flies). Fig. 147. — Venation of Dixa. {After Comstock.) Fig. 148. — Venation of an asllid {Erax). {After Comstock.) AAA. Antennae of three segments; Radius four-branched. B. Vertex of head hollowed out between the eyes; palpi present. — Asilidcc (Robber Flies). BB. Vertex of head not hollowed out; alulets small; beak prominent. — Bombyliidce (Bee Flies). Chief Families of the Cyclorrhapha (Figs. 151 and 152): A. Adults non-parasitic; maxillae covered by upper lip; Radius 3-branched. B. With a spurious longitudinal vein between Radius and Media; front convex between the antennae. — Syrphidce (Flower Flies), p. 250. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 24 1 BB. With rudimentary mouth-parts; palpi wanting; antennae with dorsal arista.— tE^^r/^o" (Bot Flies), p. 254. BBB. With well developed mouth-parts; palpi present; head with a suture above the antennae. — Superfamily Muscoidea. C. Alulets small; eyes of males not contiguous; thorax without com- plete transverse suture. — (Acalyptrate Muscids.) Rli. Miti Fig. 149. — Venation of a leptid (Leptis). {After Comstock.) Fig. 150. — Venation of a syrphid (Eris talis). (After Comstock.) D. Subcostal or auxiliary vein ending in the costa and distinctly separate from Radius I, or first longitudinal, which usually ends near the middle of the wing. Anal cell present. E. Oral vibrissae present; front bristly; R. nearly half the wing length; cross veins not close together; yellow or brown. — Scatophagidce (Dung Flies). Fig. 151. — Venation of Thereva. {After Comstock.) Fig. 152. — Venation of a muscid {Musca). {After Comstock.) EE. Oral vibrissas absent; eyes large; first posterior cell (R5) closed or narrowed in the margin; proboscis and ovi- positor greatly lengthened. — Conopidw (Thick-headed Flies). DD. Subcostal vein absent, vestigial or incomplete; Radius I usually ending in costa before middle of wing. E. Discal and basal cells united; Anal cell absent. — Os- cinidce (Grass Stem Flies), p. 260. 16 242 ECONOMIC ENTOMOLOGY EE. Discal and second basal cells separated; anal cell complete. F. Oral vibrissa present. G. Arista long plumose or pectinate above. — DrosophilidcE (Pomace Flies), p. 260. GG. Arista bare, pubescent or short plumose; front bristly as far as middle, usually light colored. — Agromyzidce (Leaf-miner Flies), p. 262. FF. Oral vibrissae absent. G. Subcostal vein abruptly bent forward before the tip of Radius I; anal cell angular. Wings pictured. — Trypetida (Fruit Flies), p. 264. GG. Subcostal vein more or less fused with Radius I; all three basal cells distinct, anal cell not produced; antennae more or less elongate and decumbent. — Psilidce (Rust Flies), p. 262. CC. Alulets or calypters large; eyes of males often contiguous; thorax with complete transverse suture. — Calyptrate Muscids. D. Cell Radius 5 closed or more or less narrowed at the margin of the wing. E. Antennal bristle bare. — Tachinidce (Tachina-flies), p. 278. EE. Antennal bristle bare near tip. — Sarcophagida (Flesh- flies). EEE. Antennal bristle pubescent or plumose to the tip. F. Dorsum of abdomen bristly; legs elongate. — Dexiidce. FF. Dorsum of abdomen not bristly except at tip. — Muscida (House-flies), p. 268. DD. Cell Radius 5 widely open. — Anlhomyiida (Root-maggot flies), P- 273- AA. Adults parasitic; upper lip enveloped by maxillae as by a sheath. — Piipipara (Sheep-ticks, etc.), p. 279. (Consult Tech. Series, No. 22, Bur. Ent., U. S. Dep. Ag. on "The Structure of Certain Dipterous Larvae, etc., " by N. Banks, 19 12) TIPULIDiE (CRANE FLIES) Meadow Maggots {Crane Flies or Leather Jackets). Adult. — Large mosquito-like flies with very long thin legs, long slender bodies, narrow wings and thread-like antennas. A transverse V-shaped suture on the back of middle portion of the thorax (Figs. 145 and 153). Larva. — When full grown about an inch long, dirty brown, and footless; of a tough leathery texture; cylindrical; tapering in front and blunt behind. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 243 Pupa. — No puparium; occupying small cells near the surface of the ground in a vertical position. Broods. — There are two broods each season. Larvae winter over and change to pupae in late May. Adults soon appear and deposit eggs from which hatch the maggots. These change to pupae and adults in September when eggs are laid for a fall brood. The maggots hatching from these eggs winter over. Control. — Early fall plowing, draining, and rotation of crops. Fig. 153.- — Tipula. A, Larva; B, cast pupal skin; C, imago. {After Folsom.) Slightly reduced. CULICID^ (MOSQUITOES) Key to The Common Genera A. Palpi in both sexes at least almost as long as the proboscis. — Anopheles. AA. Palpi in both sexes less than one-half as long as the proboscis. — Aedes. AAA. Palpi in the male at least nearly as long as the proboscis; in the female less than one-half as long. — Culex. This family includes several important economic genera, comprising many hundreds of species. The more important of these are Culex pipiens, C. pungens, Anopheles maculipennis , and Stegomyia fas data = Aedes calopus. House Mosquito {Culex pipiens Linn.). Adult. — A slender-bodied, delicate fly with gauzy wings, the. veins bearing minute scales; deep yellowish to dark brown; legs and beaks not banded; abdomen with narrow whitish bands at the base of each segment. Hibernates as adult (Fig. 154). 244 ECONOMIC ENTOMOLOGY ^SS^- — Laid at night or early morning on the surface of standing water in masses of 50 to 400. Hatch in about 24 hours. * Larva. — Large head with a pair of mouth-brushes and a tube at opposite end of body for breathing, not over four times as long as broad; antennae of moderate length with a branch about the middle, bearing a tuft of hairs. Full grown in a week; dirty white, or yellowish. Pupa. — A hunched object, floating just below the surface of the water. Duration i to 3 days. Number of broods limited only by conditions of temperature and moisture. Fig. 154. — The common house mosquito : a, male; 6, female. {U. S. Bur. Enl.) Malarial Mosquito (Anopheles maculipennis Meign.). Adult. — Dififers from Culex in being much larger, more slender and with larger legs; wings longer, and more or less spotted with brown or black, and carried flat on the back when not in use; palpi or mouth-feelers as long as the beak in both sexes. (In Culex the palpi are short in the female.) A common malaria carrier. E'ggs. — ^Laid singly on surface of water; hatch in 24 to 48 hours. Larva. — ^Larva lies flat on surface; tube very short; at first black or CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 245 grey, usually banded with white; later color harmonizes with sur- roundings. Full grown in 7 to 10 days. Pupa. — Like that of Culex but with shorter, more trumpet-shaped breathing tubes; duration about 2 days. Other species of Anopheles are: A. pundipennis and A. crucians. The Salt Marsh Mosquito (^e(/e5.yo//fa7a«5Walk.), the Swamp Mos- quito {A. syhestris Theo.) and the Irritating Mosquito (Mansonia per- turbans Walk.) are commonly met with and are annoying. On the western prairies the genus Aedes is most abundant. The eggs are laid in late summer and hatch out the following spring in the water of the melting snow. There is but one brood a year. The most common species are A. spcnccrl Theob., A. fletcheri Coq., and A. cur- rlei Coq. CECIDOMYIIDiE (GALL MIDGES) Hessian Fly (Mayetiola destructor Say). — (Consult Ent. Bull. 11, Dep. Ag., Ottawa; Bull. 116, Ont. Dep. Ag.; Cornell Bull. 194; and Fig. 155. — The hessian fly (Mayetiola destructor): i, adult female; 2, mature larva; 3, puparium or " flax-seed "; 4, seed of flax. Enlarged about 8 times. (After Criddle, Ent. Bui. 11, Dep. Agric. Can.) bulletins by Webster and Marlatt.) An introduced pest from Europe and one of the most serious enemies of growing wheat. Distributed over the wheat regions of United States and Canada. Attacks also oats, barley, rye, Agropyron spp., Bromus, Elymus and Agrostis (Fig. 155)- Adult. — A small dusky 2-winged fly, l<^ inch long, about half the size of a common mosquito; the female with a dull reddish tinge and larger than the male; legs long; wings smoky-black, covered with fine black hairs and obscurely fringed. 246 ECONOMIC ENTOMOLOGY Eggs. — Spindle-shaped, reddish and i to 50 inches long; hatch in 4 to 12 days. Larva. — A footless maggot, clear-white except for a greenish stripe down the middle; last stage of larva passed in "flax-seed" covering, and having a peculiar "breast-bone," a horny forked structure. Pupa. — Pupa case deep rich brown, like small "flax-seeds;" pupa rosy colored and with a pointed beak. Broods. — ^Two generations in fall wheat regions, and one in spring wheat regions. Criddle reports a supplementary summer brood in Manitoba, the adults appearing from late June up to middle of August. Pup£e develop which winter over. Webster (640) is of the opinion that the Hessian Fly is two-brooded even in spring wheat sections. Female lays a few, to 50 or more, eggs on upper surface of leaf about last week in August, first week in September or later, according to latitude, altitude and longitude; maggots hatch in about 4 days and move down the leaf to the stem where they embed themselves within the leaf -sheath. In about 3 weeks they change to "flax-seed" but remain as larvae until the following May, when they change to pupae. The flies emerge a few days later to lay their eggs for a new spring brood on the leaves of spring cereals. The maggot stage lasts until the third week in June, and the "flax-seed" stage until the third week in August or later, when the flies emerge (Fig. 156). Parasitized by Folygnotus, Merisus, Eupelmus, TetrasHchus, and Entedon, all Chalcids. Control. — ^Late seeding in fall on well prepared seed-bed; trap- strips; destruction of all volunteer wheat; destruction of "flax-seeds" at threshing; co-operation. Plowing the wheat stubble deeply immedi- ately after harvest. (See Part IV). Clover Seed Midge (Dasyneura leguminicola Lintner).— (Consult Bull. I 34, 111. Agr. Exp. Stn.). A widely distributed pest of red and white clover fields. Alsike, mammoth and alfalfa are uninjured. Adult. — A minute 2 -winged fly,K2 inch long, with red abdomen and long reddish-brown legs and antennae; head and thorax black; wings transparent with dusky hairs. April-May and July-August. Eggs. — Very minute, orange, smooth and transparent. Laid in green flower-heads, hatch in about a week. Larva. — A footless orange maggot, Hq mch long, and with nine pairs of respiratory tubercles and a sternal spatula. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 247 248 ECONOMIC ENTOMOLOGY Pupa. — Cocoon oval, 3^2 inch long, made of silk threads; pupa pale orange; eyes brown; two short tubercles on front of head. Life-history. — There are two broods each year. Eggs are laid in May in the forming flower-heads. At the end of June and early July (June 20 to July 8 in IlHnois) the maggots mature and drop to the ground to pupate. The adult flies emerge when the second crop of clover comes into bloom (July 15-Sept. i) and lay their eggs among the blossoms. The maggots leave the ripe heads in autumn, and pass the winter in the ground. In May the adult flies emerge to lay their eggs. Afl'ected florets do not expand their petals and remain fresh and pink until after maggot leaves the bud, eventually fadmg and withermg without opening. Natural Enemies. — Tetrastichus, Anopedius, Triphleps. Control. — Cutting or pasturing clover before the 20th of June. Clover Leaf Midge {Dasyneura trifolii Low.).- — A serious pest of white clover, affected leaves folding upon a midrib with maggots enclosed. Adult. — Smaller than the Clover Seed Midge, but very similar in color and markings. Abdomen is darker, due to the large dorsal bands of black scales. Eggs. — Colorless soon becoming orange, cylindrical and slightly curved; very minute; several eggs usually placed together between folded leaflets near the ground. Larva. — White at first, orange later; J25 inch long. Leaflet remains folded in half along the midrib. Pw^a.— Cocoon oval and about ^{5 inch long; pupa orange, with blackish eyes and a darker median ventral stripe. Life-history. — Probably four broods, each requiring about a month. Control. — Pasturing or cutting frequently. Rose Midge (Dasyneura rhodophaga). — An introduced pest of green- house roses and often does serious injury. It is known also as the Reinberg Fly by florists. The larvae "feed inside the flower and leaf buds, preventing and distorting their growth, and soon causing them to turn brown and then to blacken and die." Several generations. Adult. — A 2-winged fly with long delicate legs; 3'^o inch long. Eggs. — Cylindrical; laid at bases of the flower and leaf buds. Hatch in 2 days. Larva. — One-twelfth inch long and legless; mature in one week; CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 249 drops to the ground, burrows beneath the surface and spins a silken cocoon. Pupa. — Pupa within cocoon; duration one week. Hibernates. Control. — Frequent fumigation with tobacco to kill the adults. Grape Blossom Midge {Contarinia johnsoni Sling.). — A pest in the Chatauqua grape belt of New York. Adult. — A midge ifg inch long, with yellowish body and straw colored legs. End of May. ^i,^^- — Minute, grey, elongate, curved; about 25 laid in each bud which becomes swollen and yellowish and reddish when maggots begin to feed. Fig. 157. — The wheat midge {Diplosis trilici): a, female fly; b, male fly; c, larva. Enlarged. {After Marlale, U. S. Bur. Ent.) Larva. — Whitish to yellow-orange; }^2 inch long; passes the winter in a small oval silk-lined earthen cocoon about 6 inches below surface of ground. Pupa. — Formed at end of April. Control. — Spray with Black Leaf 40 just as buds of early varieties begin to open, and again a week later. Wheat Midge {Diplosis = Contarinia, tritici Kirby). — A European pest, destructive to wheat, introduced probably by way of the Province of Quebec (Fig. 157). Adult. — A minute orange-yellow fly Hq inch long, smoky-tinged on the back above the wings. June-August. 250 ECONOMIC ENTOMOLOGY Eggs. — Minute, cylindrical, pale red; laid singly or in clusters in crevices of wheat heads in June and hatch in about a week. Larva. — A short oval orange-yellow maggot, ^{2 inch long; as a rule it leaves the head after feeding for 3 or 4 weeks and goes into the ground where it remains in a mustard-seed-like cocoon. Pupa. — Pupa case small, about the size of a mustard seed, in the ground; formed in June shortly before the emergence of the adult. Broods. — At the end of June the adult flies lay their eggs in the crevices of the wheat head; the eggs hatch in about a week, and the larvae feed on the milky juices of the developing kernels for about 3 or 4 weeks; some descend to the ground where they form minute puparia which remam until the following June; others remam and are carried out in the screenings at threshing time. Only one brood a year. Control. — Burn or feed screenings; plow stubble deeply after harvest; rotation of crops; sow wheat early. Dry weather unfavorable and moist weather favorable for the development of the insect. SYRPHID^ (SYRPHIDS OR FLOWER FLIES) The Syrphids or Flower Flies are most valuable enemies of many injurious forms of insects. They are usually bright colored and they feed upon the pollen and nectar of flowers. Their maggots are often found in colonies of plant-lice, upon which they feed. Some syrphid larvae live in filth and are known as "rat-tailed maggots." C. L. Metcalf ("Syrphidae of Maine," Bull. 253) notes five types of Syrphid larvae: 1. The Aphidophagous type with body narrowed anteriorly, sub- cylindrical and flattened ventrally {Allograpta and Syrphus); 2. The boring type, with body nearly cylindrical (Merodon). 3. The short-tailed filth-inhabiting type {Syritta). 4. The rat-tailed filth-inhabiting type {Eristalis). 5. The Microdon type, with body hemispherical in form. Aphid-feeding species are Syrphus americanus, Allograpta obliqua, SphcBropnoria cylittdrica, Didea fasciata, S. stanthostomus (Fig. 150). The following genera live, in larval condition, in decaying vegetable or animal matter: Eristalis, Platychirius, Orthoneura, Criorhina, Syritta. (Consult "Syrphidai of Ohio" and "Syrphidae of Maine" by Metcalf.) CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 25 1 A few forms are injurious in the larval stage. The Corn-feeding Syrphid Fly {Meso gramma politus) feeds on pollen grains and at the axils of the leaves of corn, producing a wilting and browning of the lower leaves. It has been reported from several states. Merodon equestris and Eumerus strigatus are pests of the onion, narcissus and amaryUis. The larvae burrow into the bulbs. Certain species, Eristalis spp., produce myiasis in man and some of the domestic animals. The eggs are laid, singly or in masses, on or near the food upon which the larvas feed, the exact location and number depending upon the habits of the species. "They are chalk- white, shiny, elongate-ovate or subcylindrical with rounded ends, J-^s inch long and ^^^5 inch wide. Under the microscope each egg may be seen to be delicately and beautifully sculptured " The larvae vary also according to the habits of the species. They are "headless, footless, blind creeping maggots." They breathe by spiracles near the fore and hind ends of the body. They are \<2, inch long when full grown. Narcissus Fly {Merodon equestris F.). — A ser'ous pest of narcissus and daffodil bulbs in British Columbia. Adult. — A fly resembling the house-fly; March-September, most common in May, when it begins to breed. Eggs. — ^Laid in the centre of crown at surface of the ground. Larva. — Found in centre of bulb which is often destroyed. Leaves bulb in February and pupates 3-^ inch below the surface of the ground. Three-fourth to i inch length. SIMULIIDiE (BLACK FLIES, BUFFALO GNATS, TURKEY GNATS) Several species of Simulium are very troublesome pests in our northern woods, occurring in immense numbers in the vicinity of running water. The females have well developed piercing and sucking mouth-parts and their punctures are painful, with effusion of blood. Black Flies have stout black humped bodies and are small, not more than 1^ inch in length. They are most numerous in early spring and are considered by travellers worse pests than mosquitoes. They are active in the day-time, especially in bright sunshine. The eggs are laid in patches on stones or other objects under running water. The larvae are aquatic and gregarious; they are long and slender, 252 ECONOMIC ENTOMOLOGY more or less cylindrical in shape, provided at the posterior end with a disk-like sucker fringed with hooks wherewith they attach themselves to the rocks. At the anterior end are two fan-shaped organs for secur- ing food, and behind these on the ventral side is another sucker. The pupa is formed within a boot-shaped cocoon, and is provided with two tufts of respiratory filaments on the thorax. As a rule there are two or three broods in a season. The most abundant species in the northeast are Simulium venustum, S. vittatum and S. hirtipes, on the western Canadian prairies S. similis Mall. S. pictipes is innoxious. Control. — Smudges and fumes of pyrethrum as repellents; destruc- tion of larvae by phinotas oil. CHIRONOMIDiE (MIDGES) {Ceratopogon spp. {Punkies). — These minute flies, known as "pun- kies," ''no-see-ums" and ''sand-flies," are also very troublesome pests in northern woods. They are blood-suckers and attack any exposed part of the body. The larvae are thread-like and live in water or in moist places. Dr. Riley states that the following species bite: Culicoides guttipennis, the most common form; C. cinctus, C. sanguisuga, C. stellifer, C. variipennis, and C. unicolor. Not much, however, is known regarding the habits of the difi'erent species. TABANIDiE (HORSE FLIES, BULLDOGS, CLEGS, BREEZE FLIES) Common Genera: A. Hind tibise with spurs at tip; third segment of the antennae with five rings; second segment but little shorter than the first; wings with dark markings. — Chrysops. AA. Hind tibiae without spurs; third segment of the antennae with a well- developed process. — Tabanus. (Consult "Tabanidte of Ohio" by Hine) Black Horse Fly {Tabanus atratus Fab.). Adult. — A large fly with broad and slightly flattened "body and large and depressed head; last segment of antennae annulate and without stylet; females with power- ful piercing mouth-parts (see p. 8); may transmit disease (Fig. 158). Eggs. — Elongate, spindle-shaped; laid in large black masses of 500 on the leaves of grasses, sedges and other plants in marshy ground. Hatch in less than 9 days. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 253 Larva. — ^Lives in the soil, mud or water; cylindrical, tapering, 2 inches long when full grown; yellowish-white with wide dark brown bands at union of each two segments; prothorax with 2 lateral grooves on each side; mesothorax with 4 longitudinal grooves on each side; metathorax and abdominal segments like mesothorax. Carnivorous. Hibernates (Fig. 159). Pupa.— The pupal stage lasts only a few days; i}i inches long; brownish yellow; lives beneath surface of the soil. Fig. 158.- -The black gad fly. {After Carman.) Enlarged. Fig. 159. — The larva or grub of the black gad fly. {After Carman.) Treatment. — ^Protect work horses with fiy-nets; smearing ears, with a repellent solution composed of pine tar i gal., fish oil or crude carbolic acid I qt., powdered sulphur, 2 lb. On the western plains horse flies are very troublesome pests. The most common forms are T. septentrionalis Loew, T. illotus O. S., T. hirlulus Bigot, Chrysops moerens Walk., and C.fulvaster O. S. 254 ECONOMIC ENTOMOLOGY CESTRID^ (BOT FLIES) Common Genera and Species: A. Costal vein ends at tip of R4+5, M1+2 is straight not reaching the margin, and cell R5 wide open; squamae small, arista bare; ovipositor elongate. — Gasirophilus (Fig. 160). B. Wings with spots and smoky median cross band. — G. ifitestinalis. Rz*3 R-t-s Fig. 160. — Venation of wings of horse hot flies {Gasirophilus), 1, G. intestinalis; 2, G. nasalis; 3, G. hoemorrhoidalis. BB. Wings without spots. C. Posterior cross-veins (M-Cu) beyond the anterior cross-vein (r-m) ; legs blackish brown. — G. hcemorrhoidalis. CC. Posterior cross-vein opposite and nearer than the anterior cross- vein. — G. nasalis. AA. Costal vein ends at tip of M1+2; M1+2 with a bend; cell Rb much narrowed or closed. B. Facial grooves approximated below; cell Rs closed and petiolate. — (Eslrus. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 255 BB. Facial grooves far apart; squamaj large, ovipositor elongate. — Ily- poderma (Fig. 161). C. Prothoracic band of yellow hairs, mesothoracic band of brownish black hairs; media 3 sinuate; legs black with black hair; tips of hind tibiae and tarsi yellowish-brown. — H. bovls. CC. Thoracic band of hairs brownish; media 3 rounded; tibiae and tarsi yellow; femora black.: — H. lineatum. Fig. 161. — Venation I, Hypoderma linealum; 2, Warble Flies The Striped Warble Fly {Hypoderma lineatum Villers). — (Consult Bull. 5, Div. Ent., U. S. Dept. Agr.; Bull. 48, Minn. Agr. Exp. St.; Ont. Ent. Soc. Rep., 1915; Que. Soc. Prot. Plants, 1918.) Causes much loss to flesh and hides, and in lessened milk yield. Introduced from Europe. Adult. — A hairy fly resembling, a dark-colored bee; 3^^ inch long, with yellowish- white hairs; abdomen banded above with black and whitish stripes and terminated at apex with reddish-yellow hairs; thorax with four lines often seem as white by reflected light. Mouth- parts rudimentary and ovipositor blunt. Tibiae and tarsi yellow, femora black. June-July (Fig. 162). Eggs. — -Attached in spring and summer to hairs of cattle by a 256 ECONOMIC ENTOMOLOGY peculiar clasping base, often several to a hair; 3^ ^5 inch long; dull yellowish-white; narrow; ovoid. Larva. — Dr. Cooper Curtice of Washington believed that the eggs were licked into the mouth and the maggots bored through the wall of the oesophagus, whence they gradually made their way to the tissues along the back, causing warbles. Miss Ormerod, of England, on the other hand maintained the popular belief that the eggs were laid on the back, but Carpenter of Ireland, and more lately Dr. Hadwen of Canada, have proven fairly Pig. 162. — The striped warble fly {Hypoderma linealum). Enlarged. {After Hadwen.) conclusively that the eggs may be laid on almost any part of the body of the animal, and that the maggots bore into the skin where lesions and swellings are produced. They finally make their way to the back where the warbles are formed. Full grown maggots are greyish-white and nearly an inch long. When mature they make their way out through the minute opening, drop to the ground and bore an inch or so below the surface, where they change to pupae. Four stages of larva; duration 9-10 months. Pupa. — Puparium dark brown. Duration 3-6 weeks. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 257 The Ox Warble Fly {Hypoderma bovis DeG.).— This bot-fly is also European and is found in several provinces of Canada and in several states. It is more dreaded by cattle than lineaium, and causes much panic due largely to the insect's persistence and manner of egg-laying. More robust than H. lineatum. Body hairs yellow, except those on scutellum and base of abdomen which are yellowish-white, and at apex Fig. 163. — The ox warble fly {Hypoderma bovis). Enlarged. {After Hadwen.) of abdomen which are bright lemon yellow (see Table given above for structural differences between bovis and lineatum) (Fig. 163). The adults of H. bovis appeared in B. C. from May 31st to August 2d as extremes (Hadwen). Carpenter says that most of the maggots emerged from May 2 7 th to June 1 7 th. The pupal period has an average duration of about 35 days varying according to temperature. One egg is laid at a time, often when the cattle are running, besides not 17 258 ECONOMIC ENTOMOLOGY SO many laid about the hoof as with lineatiim. SwelHng is more rounded and more raised than that of lineatum, and exudes less serum. Control. — When practicable dip every lo days and treat the larvae with arsenic. Remove the larva from the warble in spring. Larvae of a species of Uypoderma have been obtained from the backs of horses. Box Flies These flies are probably of European origin but little is known of their introduction. Horse Bot Fly {Gastrophilus intestinalis DeG. = equi Fab.). Adult. — A large brownish hairy bee-like fly, % inch long; head brown with Mil^Sii. ■"T 2. 1/ Fig. 164. — Larvce of horse bot flies: i, G. hcemorrhoidalis; 2, G. inleslinalis; 3, G. nasalis. {After Dove, Bur. Ent., U. S.) three rows of black spots; wings with dark spots or bands; abdomen brown with spots and conical. July-August. Eggs. — Yellow, conical, attached by female without alighting to hairs of fore-legs, shoulders and under side of body; |f 6 inch long; hatch most readily lo to 15 days after deposition, with the aid of warmth, friction and moisture. Larva. — ^Licked into the mouth of the horse, thence into the stomach, where it attaches itself to the wall. Remains in stomach 8-10 months. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 259 In spring it escapes in the droppings to the ground and Ijores an inch or two below the surface where it pupates (Fig. 164). Pupa. — Duration 30-40 days. Chin or Nose Flies {G. nasalis Linn. andG. hcemorrhoidalis J^lnn.) . — These flies are a serious annoyance to horses in the West. They have bands of whitish, black and orange-red on the abdomen. The eggs of G. nasalis are yellowish; laid on the hairs of the throat. Parker (191 6) records the egg-laying of G. hcemorrhoidalis, the red- tailed bot fly. The egg is black, barnacle-like and stalked, and is in- FiG. 165. -An effective leather fringe device to protect horses from the nose and red-tailed bot flies. {After Dove.) serted on the hairs of the lip and nostrils by the stalk. The "striking " of the fly causes a sharp pain and excites a nervous uncontrollable fear in the horse. Control. — Administer three or four 4-oz. doses of turpentine, followed finally by an ounce of powdered aloes; stable horses in day time; groom carefully so as to kill or remove the eggs; use fly-nets of loosely dangling cords for G. equi, and wire-screen muzzles, leather nosebands cut into narrow strips or provided with canvas flaps for G. nasalis and hamorrhoidalis (Fig. 165). 26o ECONOMIC ENTOMOLOGY Sheep Bot Fly {(Estriis ovis Linn.). Adult. — A dull-yellow fly a little larger than the House-fly and covered with minute spots; abdomen with five rings, velvety and variegated with dark-brown and straw color. Antennae small ; eyes purplish-brown ; ocelli three on top of head ; no mouth; wings transparent extending beyond body ;alulets large cover- ing the poisers. June-August. Eggs. — Deposited in nostrils of sheep; hatch almost at once. Larva. — Maggot works its way up the nasal passages until it reaches the frontal sinuses, the cavities between and above the eyes. There it attaches itself and feeds on the mucus present. Young is creamy- white, with two brown spots, spiracles on last segment; full grown mag- got darker, particularly posteriorly; two small hooks on head; small rounded spots on sides of each segment. When mature, maggot passes down the nasal passages and falls to the ground, which it enters to pupate. Pupa. — Puparium smooth, hard, and black, tapering toward head; duration 40-50 days. Control. — Apply tar to the nose; furnish a shed for the sheep or a plot of plowed or dusty ground. DROSOPHILID.S (POMACE FLIES) Pomace Fly {Drosophila ampelophila Loew.). — This small fly breeds in decaying or over-ripe fruit, and is a common pest about fruit-stores. It is also suspected of being a typhoid-transmitter. The adult is a small light-brown fly with bright-red eyes; the maggot is white and about }'4 inch long; the pupa is yellow or brown with two long horn- like breathing tubes at anterior end. The front tarsus of the male has a comb of black spines on its upper side near the tip. OSClNIDiE (GRASS STEM MAGGOTS) Wheat Stem Maggot (Meromyza americana Fitch).^ — (Consult Bull. 42, Bur. Ent., U. S. Dep. Ag.) Adult. — A slender fly; yellowish-green, I5 inch long, with 3 dark stripes running down the back; femora of last pair of legs abnormally developed; eyes golden-green (Fig. 166). Eggs. — About 1-^0 inch long, and glistening white. Larva. — A watery-green footless maggot, }4, inch long, tapering to- ward front end and broader posteriorly. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 261 Pupa. — Pupa-case translucent pale green; pupa greenish and } e inch long. Broods. — Probably three generations occur each season. The eggs are laid in September-October on fall wheat. The maggots eat down into the stem where they remain all winter. In early spring they assume the pupal stage, and about the first of June the adult flies appear. This brood matures about August ist, when flies again appear. This third generation ma- tures at the end of September and the beginning of October, when the adult flies escape to lay their eggs. Besides wheat, rye, barley, and oats, this insect attacks timothy, couch grass, Elymus, Poa, and green foxtail. Control. — Grain stacked or threshed; straw stacked or burned; burning of stubble when practicable. Meromyza nigriventris Macq. and Cerodontha femoralis Meig. have been recorded as doing injury in Montana. American Grass Stem Maggot {Oscinis carbonariaLoew .) . Adult. — A black or yellowish fly, resembling a minute house-fly, ifs inch long. Larva. — A yellowish-white slender maggot with two distinct p,^ i66.-The wheat stem maggot: hook-like jaws and two knob-like a< adult; b, maggot; c, pupa; d, pupa ,11, . r i.1- within the stem; e, parasite. (After processes on the last segment 01 the i^^„„g^ ) body; ^f 2 inch long. Pupa. — Pupa- case cigar-shaped and pale chestnut brown. Broods. — Similar in life-history to Wheat Stem Maggot. The larva destroys the centre of the young shoot at the ground in the autumn. Other Species. — O. coxendix Loew. and 0. dorsala Loew. occur on prairie grasses, sometimes very abundant. 262 ECONOMIC ENTOMOLOGY Control. — Summer-fallow grass lands; prevent volunteer growth in autumn. PSILIDiE (RUST FLIES) Carrot Rust Fly {Psila roscB Fab.).- — This fly is a native of Europe, and the larva frequently does considerable injury to the roots of carrots, celery and parsnips. Adult. — One-sixth inch long, dark green, sparsely clothed with yellow hairs; eyes black, and head and legs pale yellow. Eggs. — Deposited by female about roots of host through cracks in the ground. Larva. — Maggot dark brown, ^fo inch long, slender, truncate at posterior end; segments well marked, head small. Pupa. — Puparium dark brown; anterior segment obHquely trun- cate; \i, inch long; pupation in the earth. Life-history. — (Consult Fletcher's Reports and Bull. 2>Zy U. S. Div. Ent.) Winters as larva or pupa; adults appear early in the season; summer generations develop in 3 or 4 weeks (Curtis); both flies and maggots found throughout the warmer months; number of broods uncertain. Control. — Spray the carrots four or five times at intervals of a week or ten days with kerosene emulsion, the first application at the time of thmning; spread the earth in which carrots have been stored in the poultry yard; sow late and practice rotation of crops. AGROMYZID^ (LEAF MINER FLIES) Marguerite Fly {Phytomyza chrysanthemi Kowz.). — (Mass. Agricul- tural Experiment Station, Bull. 157.) Attacks compositous plants and is especially injurious in the greenhouse. Occurs in the Northern States, and has done considerable injury in B. C. Adult. — A small greyish fly }{2 inch long, with a yellow stripe on each side of abdomen; face yellow; antennae black; legs black with yellow markings; rather inactive. Average length of generation about ;^T, days; several generations a season in greenhouse. Eggs. — ^Laid singly in incisions between flesh and skin of leaf. Hatch in 5 days. Larva. — Burrows in the leaf, producing irregular whitish lines or CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 263 patches, often causing withering, also preventing flowering or reducing the number of blossoms. Matures in about 17 days. Pupa. — Formed in larval mine. This stage lasts about 14 days; puparia dark brown. Control. — A solution of Black Leaf 40 and Soap applied at intervals of 10 or 12 days, as soon as first signs of operation of the insect. Asparagus Miner (Agromyza simplex Loew.). — ^(Consult Bull. 66, Part I, U. S. Bur. Ent.) Injures asparagus stalks, the maggot mining beneath the epidermis, sometimes girdling the stem. Adult. — A black two-winged fly; eyes and head prominent; wings clear with }q inch expanse. Probably two generations, June and August. Eggs. — -White; deposited just beneath epidermis of stalk. Larva. — -Milk-white; 3^^ inch long; footless, truncate posteriorly and tapering anteriorly. Pupa. — Puparium flax-seed-hke, red, i^f inch long; attached to slits in epidermis of asparagus stalk near ground. Control. — Pull up and burn infested stalks in spring; destroy volunteer trap plants in late June. Com or Spike-homed Leaf Miner (Cerodonta dorsaUs Loew.). — (Consult Bull. 432, Bur. Ent., U. S. Dept. Agr.) This leaf-miner has a wide distribution in the U. S. and feeds on a wide range of cereal and grass plants. Three generations at least in Indiana. Adult. — One-twelfth to 3^fo ii^ch long; proboscis, palpi, front, antenn£e, legs, mesonotum and abdomen mostly yellow. Punctures the leaves, in some of which an egg is laid. May in Indiana, but active throughout the year in Pasadena, Cal. £gg5.— Elongate, kidney-shaped, rounded at each end. Color opaque white; }-qq inch long. Hatch in 3-12 days. Larva. — ^Dirty-white; ^-q inch long; slender, nearly cylindrical; mouth-hooks black; body segments plain; posterior ends truncate; mines in the leaves and stem of host plant, frequently killing the parts affected. Full grown in 9-24 days. Pupa. — White at first, turning yellow and dark later. Duration 9-24 days. Hibernates (in Indiana). Control. — -(i) Summer fallowing, (2) fall plowing, (3) burning dry grasses along fence lines, roadsides, etc. in late fall and early spring. 264 ECONOMIC ENTOMOLOGY TRYPETIDiE (FRUIT FLIES) Common Genera (after Williston) : A. Bristle on each side of front with a terminal leaf-like appendage. — Ceralitis. AA. Front without such bristles; wings with colored markings not reticulate; scutellum not with six bristles; fourth longitudinal vein not conspicuously curved forward at its extremity. B. Distal portion of wings marked with two hyaline indentations. Sepa- rated by a curved or arched brown projection from the brown oblique cross-band; body short; abdomen as broad as thorax; antepenultimate section of fourth vein curved. — Epochra. BB. Wings not marked as in B. C. Coloring of body generally light, never black; cross-bands on wings nearly transverse; cross-veins but little oblique. — Trypeta. CC. Coloring of body black; wings with four very oblique black cross- bands; cross- veins not approximated; scutellum with 4 bristles, yellow. — Rhagoletis. Mediterranean Fruit Fly (Ceratitis capitata Wied.). — (Consult Circ. 160, U. S. Div. Entomology.) Probably a native of the East Indies. The appearance of this destructive insect in Hawaii has alarmed the fruit-growers of the Pacific coast, and quarantine restrictions have been enforced. It already occurs in Africa, Europe and Asia, in Australia and in Brazil, and attacks nearly all kinds of fruits. Adult. — An active fly about size of house-fly, ochre yellow color; eyes reddish purple; a blackish blotch in centre of forehead where two stout black bristles arise; thickened basal antennal joints yellow, terminal segments black; dorsum of thorax convex, yellowish- white marbled with shiny black blotches. Wings broad and semi-opaque with extreme base blotched with ochreous or brownish yellow, the rest of the basal area marked with black; beyond a broad, irregular, trans- verse ochreous band blotched at extremity; another similar blotch inside of costal vein. Abdomen oval, with fine scattered bristles on upper surface, and two rather broad transverse silvery white bands on basal half. Num- ber of broods depends on temperature and food supply. Eggs. — Glistening white eggs placed beneath skin of ripe fruit by sharp extensile ovipositor. Eggs not all deposited at once. LarvcB. — ^Begin feeding at once on the pulp, when mature (2-3 weeks) they leave the fruit and enter the ground, changing to puparia. Pupa. — Duration 12-21 days. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 265 Control. — Cleaning up and destruction of all fallen fruits; covering trees with netting; using a poison bait spray (Berlese and Mally). Currant Fruit Fly [Epochra canadensis Loew.)- — (Consult Bull. 264, Maine Agr. Expt. St.) A common pest on currants and gooseberries in Canada and the Northern States, and confined to the Canadian, Transition and Upper Austral zones. Adult. — Pale yellowish, slightly smaller and more delicate than the house fly; eyes green, legs yellow, wings cross-banded; active and restless. May and June. Mating period 2)2> days; preoviposition period 6-10 days. One brood a year. Eggs. — Elongate, oval, whitish, },^^ inch long; placed under skin of fruit by long ovipositor. Female may lay about 200 eggs. Hatch in 4-7 days. Larva. — Burrows within the fruit, destroying seeds and kernel. Infested berries show discolored spots, become deformed and usually fall early. Matures in 3 weeks; J^ inch long, white with black mouth- parts. Leaves the fruit and enters the ground to pupate. Pupa. — ^Puparium broadly oval and straw colored, in the ground. Hibernates. D uration lo-ii months. Control— kWov^ poultry to run ^^''- ]^l-~^ ^^"\^l^ white-banded ^ . -^ cherry fruit fly. Much enlarged. among the bushes to pick up fallen {After Caesar.) infested fruit; spray bushes with a sweetened poison of sodium arsenite and diluted molasses to kill adult flies at intervals of a week beginning early in May. A heroic but effectual method is to pick entire crop of fruit and destroy it before the maggots emerge. White-banded Cherry Fruit Fly {Rhagoletis cingulata Loew.). Adult. — A small blackish fly, smaller than the House-fly, % inch long, expanding % inch; pale yellow spot on hinder part of thorax and a yellowish stripe along each side of thorax; head yellow, eyes gold-green; legs yellow, abdomen crossed with 3 or 4 white bands. Wings with four brown cross bands, and a black spot at tip. June (Fig. 167). Eggs. — Egg-laying begins about 11 days after emergence of flies. 266 ECONOMIC ENTOMOLOGY Eggs inserted under the skin of cherries; small, glistening white; ellip- tical; hatch in about 5 days. Larva. — One-fourth inch long, white or cream-colored, cyhndrical, tapering. Twelve to 22 days in fruit; destroys the pulp. Leaves the cherry when full grown. Pupa. — Puparium formed just beneath the surface of the ground; brown; hibernates. Black-bodied Cherry Fruit Fly {Rhagoletis fausta O. S.). — (Consult Bull. 227, O. A. C, 1915.) Adult. — Larger than preceding; black with- out white cross-bands on the abdo- men; head, eyes and legs similar to those of cingulata but bands on wings darker and differently arranged (Fig. 168). Eggs and Larva. — Similar to those of cingulata. Pupa. — Puparium cream or straw colored. Control. — Spraying with sweet- ened arsenate of lead solution (2 to 3 lb. arsenate of lead (paste), 40 gal. of water and i gal. of cheap molasses) when the flies begin to emerge about June loth, and again 10 to 12 days later. Apple Maggot or Railroad Worm {Rhagoletis pomonella Walsh). — (Consult Rep. Maine Ag. Exp. St., 1889; Cir. loi. Bureau of Ent., U. S. Dep. Agr.; Bull. 171, N. H. Ag. Exp. St.; Bull. 324, Cornell Ag. Exp. St.; U. S. Dep. Ag., Bull. 9.) This maggot is a serious pest of apples in N. E. districts. It is probably a native species, and occurs widely in both the United States and Canada on apple, crab- apple, haw, and huckleberry. Perhaps most common on sweet and sub-acid varieties of apple. Adult. — A small fly, a little smaller than the house-fly; blackish, with yellow head and legs; eyes green; 3-4 white bands (3 in male and 4 in female) across the abdomen; wings marked by four dark irreg- ular bands. July and later, each female capable of laying 300-400 eggs; uses sharp ovipositor to puncture the skin of the fruit. Pre- oviposition period may be as short as one week or less, but usually longer than a week (Fig. 169). Fig. 168. — A female black-bodied cherry fruit fly. Much enlarged. {After Caesar.) CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 267 Eggs. — Elliptical, yellowish, pedicellate, ^^q inch long; laid singly just under the skin of the apple; hatch in 4-10 days. Larva. — ^A small plump white legless maggot, l^ inch long; mouth- parts with a pair of small black rasping hooks; caudal end truncate; Fig. 169. — A female of the apple maggot fly {Rhagoletis pomonella). M uch enlarged. {After W. H. Briltain.) makes soft discolored trails and corky strands in the pulp; full grown in 4-6 weeks, or when the infested fruit is ripe. • Infested apple usually falls, and larvae leave the fruit i to 4 weeks later to enter the ground (Fig. 170). Fig. 170. — A parasite of the apple maggot (Biosteres rhagoletis). Enlarged. W. H. Briltain.) {After Pupa. — -Puparium just beneath the surface of the ground in which the pupa rests all winter, and in some cases the following year. Some flies emerge in September from early pupae. 268 ECONOMIC ENTOMOLOGY Life-history. — Hibernates as pupa in the ground; adults begin to emerge in July, and appear irregularly later; maggots hatching from the eggs tunnel in the flesh of the fruit, sometimes close to the surface. They mature in 4-6 weeks, and make their way out of the apple to the ground, the time (i to 4 weeks) depending on variety of apple — a short time (3 days) in early apples. Infested fruit usually falls. There is but one generation each year. " Some forms require an extra year for the pupal stage" (O'Kane). Control. — Apply arsenical or poison-bait spray in early July for adults; collect fallen apples; allow hogs the run of the orchard. Records Locality Emergence of adults Oviposition Larval period Second brood adults Authority Ithaca, N. Y. . . Durham, N. H.. Bowmanville, June IS 1910, July 9 191 1, June 26 1912, June 28 1913, July 10 191 2, July 6- Aug. 20 1915, July 27 —Sept. 29 1916, July 18 -Sept. 18 July 4 July 4- Sept. 18 July 20 July 27-Sept. II July 25-Sept. 12 July 4 (12-32 days) 30 days more or less Some flies emerge in Sept, None Illingworth O'Kane. Ont. Windsor, N. S... 4 weeks + None Brittain MUSCIDiE (MUSCLDS) Common Genera (Figs. 171 and 172): A. Proboscis long, slender, directed forward, adapted for piercing; arista pectinate (rays on one side only). B. Palpi nearly as long as proboscis. — Hamatobia (Lypcrosia). BB. Palpi much shorter than proboscis. — Stomoxys. A A. Proboscis not elongate; labella fleshy and not adapted for piercing. B. Arista plumose; hypopleurae with a vertical row of bristles; eyes bare; vibrissal angle distant and above oral margin. C. Thorax and abdomen with depressed yellow woolly hairs among the bristles; sternopleurals arranged i : i. — Pollenia. CC. Thorax and abdomen without such hairs; sternopleurals arranged 2:1; mesonotum distinctly striped; bright metallic. — Chryso- myia. BB. Arista plumose; hypopleura; without a row or tuft of bristles. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 269 C. Last section of fourth vein (Mi^.2) with a rounded angle. — Musca. CC. Last section of fourth vein curved forward, often slightly, beyond / d.dc anterior dorso centrals aide •■ inner - a. ia ■■ intraalar h liumerals p.h post " * '\ps. presutural Scute Hum hdc posterior dorso centrals yp.ldc ■• inner •• i.a. intraalar pra prealar = anterior sa sa supra alar -.. sq. \ -( Lower squamar \jj isq.\ \ ^^'\squamula thoracal is ■ ^ \5quamula a/aris Vertical -Ocelli prbitals • --•- •---.-- \^ ^Transi/erse suture , , a. Ida. ...Pjdc a.dc — • • >./) 2/4,.. }.^-- ./^53, ■Ocellar Antenna r^lil^^-Vibrissal ndges Oralmargin Vibrissa ^Palpus Proboscis Fig. 171. — Dorsal aspects of the thorax, and frontal aspect of the head of a muscoidean fly, with designations of the parts commonly used in taxonomic work. {After Riley and Johannsen, Comstock Pub. Co., Ithaca, N. Y.) its middle or at the tip, the cell broadly open; the first longitudinal vein (Ri) ending beyond the middle of the wing. — Muscina. BBB. Arista plumose; hypopleurae and eyes as in B; vibrissal angle, near oral margin. 270 ECONOMIC ENTOMOLOGY C. Mesonotum flattened behind the transverse suture; posterior dor- socentral and acrostichal bristles inconstant and unequally developed. — Phormia. CC. Mesonotum not flattened behind the transverse suture; posterior dorsocentral and acrostichal bristles well developed and constant. D. Cheeks hairy; third longitudinal vein {Ri^b) spinulose at base only. — Calliphora. DD. Cheeks bare; third longitudinal vein (R4+5) spinulose.— Lucilia. .Trans verse sutur ,Post alar callus Propleura- Front coxa -^ Haltere Hind coxa Middle coxa- Fig. 172 — ^Lateral view of the thorax of a muscoidean fly, with designations of the parts commonly used in taxonomic work. {After Riley and Johannsen.) House-fly {Musca domestica Linn.). — A cosmopolitan insect dangerous to human life. A carrier for typhoid fever, tuberculosis, dysentery and other diseases (Fig. 173). Adult. — A two-winged fly with four black hnes on back of thorax; bristle of antennae feathered; vein ending near tip of wing distinctly elbowed; no bristles on abdomen except at the tip. Mouth-parts used for sucking not for piercing, retractile; mouth-parts and feet specially adapted for carrying micro-organisms. Each foot with two claws and two sticky pads. Egg-laying begins 10-14 days after adult emerges from puparium (Fig. 174). Eggs. — Minute, glistening white, long ovoid, }^ inch long. Laid in irregular small clusters. Each female lays about 120 eggs at a time CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 271 and may lay several times; hatch in about 8 hours in mid-summer. Laid in horse manure, pig manure, and to a less extent in other manure, human excreta, in decaying grain, moist bran, moist mixtures of hay and grain from feed troughs, in excreta-soiled straw, decaying kitchen refuse, rotting fruits, vegetables, in ensilage. Fig. i73.^The common house-fly (Musca doynesticd) . Puparium at left; adult next; larva and enlarged parts at right. All enlarged. {After Howard.) Larva. — At first glistening white; two moults; duration about 5 days; yellowish when full grown, slender in front and truncate behind; a large hook above the mouth; active. Develops in horse manure and other filth in substances more or less alkaline. ^ Pupa. — ^Puparium nearly cylindrical, dark chestnut; duration 3-4 days. Duration of Hfe-cycle 10-14 days. Prob- ably seven to ten generations develop be- tween April 15th and October loth. It hibernates as larva or pupa in the South but probably more commonly as adult in the North. (Consult Howard's and Hewitt's books on "House Flies.") Stable Fly {Stomoxys calcitrans Linn.). — Occurs in stables, yards, shady groves, dwellings, etc. Adult. — Resembles house-fly, but has piercing mouth-parts; bright golden tinge at front end of median, light stripe on thorax; six black lines on thorax; dorsal surface of abdomen with a number of nearly round dark spots. Bite severe but not poisonous. A carrier of disease; breeds in moist straw and hay. P e Fig. 174. — Extremity of tarsus: e., empodium; p., pulvillus in A, Bibio; B, Musca. 272 ECONOMIC ENTOMOLOGY Eggs. ^Laid in an irregular heap of about 100 on manure and gar- bage; similar in form to those of House-fly; hatch in 2-3 days. Larva. — Similar in form to that of House-fly, but more trans- lucent in appearance. Duration 10-20 days. Pupa. — Duration 6-20 days; puparium reddish-brown, elongate- oval, }i inch long. This fly occurs in the open, but often enters houses; breeds rapidly in oat-straw and other organic refuse. Winters as pupa or larva. Control. — Apply 0.62 lb. borax to every 10 cu. ft. (8 bushels) manure, on removal from stables, with a flour sifter or fine sieve, particularly about the edges of the pile, and sprinkle 2 or 3 gal. water over the heated manure; use fly-traps. (Consult Farmers' Bulls. 540, 734 and 851, U. S. Dep. Agr., 1913.) Horn Fly {Hcematobia serrata ^oh. -T>es,v.,Lyperosia irritans'Lm.n.) . — (Consult Circ. 115, Bur. Ent., U. S. Dep. Agr.) Introduced into U. S. about 1886 from Europe, and has spread rapidly since. Adult. — Similar in shape and color to House-fly, but about half as large. June-September. Eggs. — ^Laid singly in fresh cow manure in day time, irregular, oval, light reddish brown. Egg-laying begins soon after adult emerges. Larva. — White, 14 i^^ch long; full grown in 4-6 days. Pupa. — Puparium dark brown, ellipsoidal, 36 i^^h long; pupal stage lasts 5-10 days. Probably 6-8 generations in a season. Control. — (i) Killing the maggots by the introduction into the man- ure of Hme and other drying and destructive agents; (2) application of creolin compounds in the form of spray, or kerosene emulsion solution, or a mixture of 3^^ gal. fish oil, Yi pint coal oil, 4 tbspfls. crude carbolic acid applied with a cloth rubbed over the parts attacked. The main factors limiting the number of the common flies are: (a) The destruction of the larvae and pupae by braconid and chalcid parasites; {h) The lack of food for the larvae; (c) The enemies of the adults; {d) Weather conditions — oppressive sultry weather; cold, wet and windy weather; acting on the adults, and preventing the emergence of adults from the pupae. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 273 The Screw-worm Fly {Chrysomyia macellaria Fab.) occurs as far north as Canada but is of importance economically in the south- western States as a pest of stock. The adult is larger than the house-fly, of a dark bluish-green color, with three distinct black stripes on the thorax. The eggs are laid in irregular masses upon dead animals and in wounds. The maggots bore into the carcass or flesh, often causing death. (See Farmers' Bull. 857, U. S. Dep. Ag.) Blue Bottle or Green Bottle Flies. — -Two or three common species of these flies occur which are also known as Blow, Green or Blue Bottle FHes. Meat Fly, or Blue Bottle, or Blow Fly {Calliphora vomitoria Linn.). — • A large blackish fly with bluish abdomen and black spines on the thorax. Its eggs are laid on meat and dead animals, and each female may lay 400 to 600 eggs, which hatch very soon after deposition. Duration of a gen- eration 22 to 23 days. C. erythrocephala Meig. is another common species with a pre-oviposition period of 12-17 days, an active larval stage of 3-4 days and a pupal stage of 7-9 days. Green Bottle Fly (Lucilia ccBsar Linn.). — Similar in habits to Meat Fly, with pre-oviposition period of 1-3 weeks, active larval stage of 2-5 days and a pupal stage of 5-16 days. Hibernates as larva and pupa. Phormia regina Meig. is a large black fly seen in early spring in houses, and breeds in garbage. Large Blue Bottle Fly {Cynomyia cadaverina Desv.) frequents pantries. Lays eggs on meats — smoked, uncured and cooked. Pre- oviposition period i to 3 weeks, larval period 5-40 days, and pupal stage 1-8 weeks. The Cluster Fly {Pollenia rudis Fabr.) and Muscina stabulans Fall, are also dangerous as disease carriers (see Part I). The former is found in early spring and late autumn crawling sluggishly about, often collecting in large numbers in and about houses. It has short curly yellow hair on dorsum of thorax. Probably breeds in manure and garbage. ANTHOMYIDiE (ANTHOMYIDS) Root Maggots {Phorbia spp.). — Three spec'es of root maggots are commonly injurious to root crops — Cabbage Root Maggot, Onion Maggot and Seed Corn Maggot. Cabbage Root Maggot {Phorbia brassicce Bouche). — A widely dis- tributed insect, introduced from Europe. 18 2 74 ECONOMIC ENTOMOLOGY Adult. — Smaller than House-fly; He inich long; greyish, with three blackish, rather broad bands on back of thorax and a dark stripe along back of abdomen; a number of stiff hairs on body and legs; eyes red- ) /"^ t/i' V ■ # ''\^J Fig. 175. — Male of the cabbage root maggot fly. Enlarged about 3 times. (Photo by J. T. Wadsworth. After Gibson and Treherne, Bui. 12, Ent. Br. Dept. Agric. Ottawa.) Fig. 176. — Female of the cabbage root maggot fly,. Enlarged about 3 times. (Photo by J. T. Wadsworth.) After Gibson and Treherne, Bui. 12, Ent. Br. Dept. Agric. Ottawa.) dish-purple. Hibernates sometimes as adult. Pre-oviposition period about 6 days (Figs. 175 and 176). Eggs. — Elliptical, white, ^^5 inch long; 50-60 deposited separately on the surface of ground or on stem of plant; stage lasts about a week. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 275 Larva. — A whitish, cylindrical, footless maggot, tai)ering toward the front, and abruptly terminated behind, where are 12 two-pointed fleshy tubercles and 2 conspicuous reddish-brown spiracles; 3^:4 inch long when full grown (3 to 4 weeks) (Figs. 177 and 178). Pupa. — Puparium in earth, oval, 3^^ inch long, chestnut-brown; 2 weeks in June; hibernates. Pig. 177. — (a) Caudal end of cabbage root maggot; {h) of the imported onion maggot; and (c) of the seed-corn maggot; showing arrangement of fleshy tubercles and central spiracles. All much enlarged. {After Gibson and Treherne, Ent. Bui. 12, Dept. Agric. Ottawa.) Life-history. — Adults appear in May, when cabbages are being set out, and deposit eggs. Maggots hatch in a week and feed on roots for 3 or 4 weeks when they change to pupae within puparia in the soil. In 15 days or so the adults appear in late June and July to lay eggs for a second brood. The number of broods is uncertain, probably three or four, but the later broods do but little harm. Fig. 178. — Cabage root maggot, side view. Enlarged 7 times. {After Gibson and Treherne, Ent. Br. Can.) Control. — Use "single-ply tarred felt" paper disks when young plants are set out; use cheese cloth frames as screens; plant trap-crops; apply white hellebore or pyrethrum either as dust or as solution; use carbolic wash; use corrosive sublimate solution (4 oz to 50 gal. water). In the case of the last three insecticides, treatment should be made when the plants are set out and repeated once a week for 5 weeks. Enemies. — Baryodma ontarionis, a Staphylinid; Cothonaspis gillettei Wash., a Cynipid; and Trombidium spp. — (Consult Bull. 12, Ent. Br. 276 ECONOMIC ENTOMOLOGY Dep. Agr. Canada, 1916; Bull. 419, N. Y. Agr. Exp. Stn.; Cornell Univ., Bull. 78.) Onion Maggot {Phorbia ceparum Mg. = Hylemyia antiqua Mg.). Adult. — Slightly larger than Cabbage Root Maggot Fly; body and legs with many black bristles; back of thorax of male with four indistinct dark colored bands; abdomen with a distinct blackish band down the middle; May-June. Probably three broods a year. Pre-oviposi- tion period about 10 days (Fig. 180). Fig. 179. — Onion maggot (Phorbia ceparum), female and head of male. Eggs. — Cylindrical, white, distinctly ridged; groove not so deep or long as in P. brassicce; duration 3 to 4 days. Larva. — White, cylindrical, rounded, truncate at posterior end; ^5 inch long; central tubercles of blunt end single-pointed, with a pair of additional tubercles. Duration 2-3 weeks, occasionally 4-5 weeks. Young larva works its way down within the sheath of the plant to the forming bulb, in which it feeds. Pupa. — Puparia formed in soil or in outer layers of onion. Found 13^^-3 inches below the surface. Summer duration about 2 weeks; hibernates. CLASSIFICATION AND DESCRIPTION OF COMMON INSECTS 277 The Barred-winged Onion Maggot {Chaitopsis oenea Wied.) is also injurious to onions (Michigan). Control. — Apply poisoned bait spray composed of sodium arsenite and molasses to kill adults; apply hellebore, pyrethrum and carbolic wash. Seed Com Maggot (PhorbiafuscicepsZett.). — (Consult Bull. 12, Ent. Br. Dep. Agric. Can.). Injurious frequently to beans, peas and corn. Adult. — Smaller than Onion Maggot Fly, }-^ inch long; bands on back of thorax indistinct, those on abdomen distinct; inner side of pos- terior tibiae of male with a row of short bristly hairs. Body of female pointed, eyes widely separate. June-July. Eggs. — ^Laid on or about the seed in the soil, or on the seedling. Larva. — Smaller than Cabbage Root Maggot or Onion Maggot, 3^^ inch long; whitish, cylindrical, footless, blunt at caudal end and pointed at the head. Caudal tubercles simple, rather close together with a trace of additional tubercles. Feeds mostly on the seed. Pupa. — Puparium }i inch long, light brown to dark reddish-brown; duration 12 days. Number of generations not yet known. Injury seems most severe when a wet period follows immediately after planting the seed. Control. — Difl&cult. Use mineral fertilizers; carbolic acid emulsion. Raspbeny Cane Maggot (Phorbia rubivora Coquillet). Adult. — A grayish-black fly, smaller than the house-fly. April. Eggs. — White, elongate, 3^^ 5 inch long, laid in the axil of young leaves at the tip of shoot. Hatch in a few days. Larva. — Maggot bores into the pith of the shoot, and tunnels downward, making a tortuous path. About halfway down it girdles the wood beneath the bark. It continues burrowing downward and becomes full grown in June. Wilting occurs in May. Pupa. — Formed at lower end of burrow in June and July. Control. — Cut off and burn the wilting canes as soon as observed. Beet Leaf Miner {Pegomyia vicina Lintner). — It is sometimes de- structive to beets in late fall. Whitish blotches are formed on the leaves. There are several generations each year, and the winter is passed in the pupal condition under fallen leaves or in the soil. The eggs are placed on the lower side of the leaves, and the maggots mine in the leaves; life-cycle about a month. Control. — Pick and burn infested leaves where practicable; use 2 78 ECONOMIC ENTOMOLOGY spinach as a trap crop; plow deep and harrow as soon as crop is removed. Lesser House-fly {Homalomyia canicularis Linn.). — This fly is smaller than Musca domestica, and may be observed in houses in early summer. As an Anthomyiid it can be readily distinguished from the true muscids by